SK51072007A3 - Zlepšený spôsob prípravy kaprolaktámu z nečisteného 6-aminokapronitrilu - Google Patents

Zlepšený spôsob prípravy kaprolaktámu z nečisteného 6-aminokapronitrilu Download PDF

Info

Publication number: SK51072007A3
Authority: SK; Slovakia
Prior art keywords: caprolactam; acn; water; column; boiling
Prior art date: 2005-03-18

Application number

SK5107-2007A

Other languages

English (en)

Slovak (sk)

Inventor

Alan M. Allgeier

John J. Ostermaier

Sourav K. Sengupta

Original Assignee

Invista Technologies S. A. R. L.

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2005-03-18

Filing date

2006-03-15

Publication date

2008-12-05

2006-03-15 Application filed by Invista Technologies S. A. R. L. filed Critical Invista Technologies S. A. R. L.

2008-12-05 Publication of SK51072007A3 publication Critical patent/SK51072007A3/sk

Links

JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 title claims abstract description 271
238000000034 method Methods 0.000 title claims abstract description 49
KBMSFJFLSXLIDJ-UHFFFAOYSA-N 6-aminohexanenitrile Chemical compound NCCCCCC#N KBMSFJFLSXLIDJ-UHFFFAOYSA-N 0.000 title claims abstract description 20
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 72
238000009835 boiling Methods 0.000 claims abstract description 70
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims abstract description 70
238000004821 distillation Methods 0.000 claims abstract description 67
239000003054 catalyst Substances 0.000 claims abstract description 34
239000007788 liquid Substances 0.000 claims abstract description 33
238000005984 hydrogenation reaction Methods 0.000 claims abstract description 28
ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 claims abstract description 23
239000012808 vapor phase Substances 0.000 claims abstract description 19
239000001257 hydrogen Substances 0.000 claims abstract description 10
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 10
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 9
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 67
229910021529 ammonia Inorganic materials 0.000 claims description 32
230000018044 dehydration Effects 0.000 claims description 26
238000006297 dehydration reaction Methods 0.000 claims description 26
239000000126 substance Substances 0.000 claims description 23
239000000203 mixture Substances 0.000 claims description 20
238000006243 chemical reaction Methods 0.000 claims description 13
239000007795 chemical reaction product Substances 0.000 claims description 7
NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 4
238000001816 cooling Methods 0.000 claims description 3
239000000945 filler Substances 0.000 claims description 3
229910052751 metal Inorganic materials 0.000 claims description 3
239000002184 metal Substances 0.000 claims description 3
150000003624 transition metals Chemical class 0.000 claims description 3
150000002739 metals Chemical class 0.000 claims 1
229910052723 transition metal Inorganic materials 0.000 claims 1
238000004519 manufacturing process Methods 0.000 abstract description 10
SCEIUGQQBYRBPP-UHFFFAOYSA-N 2,3,4,5-tetrahydro-1h-azepine Chemical compound C1CCC=CNC1 SCEIUGQQBYRBPP-UHFFFAOYSA-N 0.000 abstract description 6
125000005219 aminonitrile group Chemical group 0.000 abstract description 6
238000007363 ring formation reaction Methods 0.000 abstract description 6
150000003951 lactams Chemical class 0.000 abstract description 5
230000003301 hydrolyzing effect Effects 0.000 abstract description 4
239000000047 product Substances 0.000 description 26
238000010992 reflux Methods 0.000 description 21
239000000463 material Substances 0.000 description 13
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
230000015572 biosynthetic process Effects 0.000 description 10
238000012856 packing Methods 0.000 description 9
238000012546 transfer Methods 0.000 description 9
241000282465 Canis Species 0.000 description 8
MHCVCKDNQYMGEX-UHFFFAOYSA-N 1,1'-biphenyl;phenoxybenzene Chemical compound C1=CC=CC=C1C1=CC=CC=C1.C=1C=CC=CC=1OC1=CC=CC=C1 MHCVCKDNQYMGEX-UHFFFAOYSA-N 0.000 description 6
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 6
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
239000012535 impurity Substances 0.000 description 6
KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
238000000746 purification Methods 0.000 description 6
238000009833 condensation Methods 0.000 description 5
230000005494 condensation Effects 0.000 description 5
239000000539 dimer Substances 0.000 description 5
238000010438 heat treatment Methods 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
239000013529 heat transfer fluid Substances 0.000 description 4
239000003921 oil Substances 0.000 description 4
229910052763 palladium Inorganic materials 0.000 description 4
229910052697 platinum Inorganic materials 0.000 description 4
238000003786 synthesis reaction Methods 0.000 description 4
SCHOATXEWOOTHN-UHFFFAOYSA-N 3-aminohexanenitrile Chemical compound CCCC(N)CC#N SCHOATXEWOOTHN-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
229920002292 Nylon 6 Polymers 0.000 description 3
BTGRAWJCKBQKAO-UHFFFAOYSA-N adiponitrile Chemical compound N#CCCCCC#N BTGRAWJCKBQKAO-UHFFFAOYSA-N 0.000 description 3
238000004458 analytical method Methods 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
230000003197 catalytic effect Effects 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
238000000926 separation method Methods 0.000 description 3
239000000243 solution Substances 0.000 description 3
229910001220 stainless steel Inorganic materials 0.000 description 3
239000010935 stainless steel Substances 0.000 description 3
230000003068 static effect Effects 0.000 description 3
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
229910052921 ammonium sulfate Inorganic materials 0.000 description 2
235000011130 ammonium sulphate Nutrition 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
239000011575 calcium Substances 0.000 description 2
229910052804 chromium Inorganic materials 0.000 description 2
239000011651 chromium Substances 0.000 description 2
229910052802 copper Inorganic materials 0.000 description 2
239000010949 copper Substances 0.000 description 2
VEZUQRBDRNJBJY-UHFFFAOYSA-N cyclohexanone oxime Chemical compound ON=C1CCCCC1 VEZUQRBDRNJBJY-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000012530 fluid Substances 0.000 description 2
238000004817 gas chromatography Methods 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
-1 lactam sulfate Chemical class 0.000 description 2
229910052744 lithium Inorganic materials 0.000 description 2
229910052749 magnesium Inorganic materials 0.000 description 2
239000011777 magnesium Substances 0.000 description 2
229910044991 metal oxide Inorganic materials 0.000 description 2
150000004706 metal oxides Chemical class 0.000 description 2
229910052750 molybdenum Inorganic materials 0.000 description 2
239000011733 molybdenum Substances 0.000 description 2
229910052759 nickel Inorganic materials 0.000 description 2
239000005416 organic matter Substances 0.000 description 2
239000008188 pellet Substances 0.000 description 2
230000000737 periodic effect Effects 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000011591 potassium Substances 0.000 description 2
239000002243 precursor Substances 0.000 description 2
239000000376 reactant Substances 0.000 description 2
229910052703 rhodium Inorganic materials 0.000 description 2
239000010948 rhodium Substances 0.000 description 2
229910052710 silicon Inorganic materials 0.000 description 2
239000010703 silicon Substances 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
229910052719 titanium Inorganic materials 0.000 description 2
239000010936 titanium Substances 0.000 description 2
239000004408 titanium dioxide Substances 0.000 description 2
229910001935 vanadium oxide Inorganic materials 0.000 description 2
101710199735 2-methylcitrate dehydratase Proteins 0.000 description 1
SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
101710159080 Aconitate hydratase A Proteins 0.000 description 1
101710159078 Aconitate hydratase B Proteins 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
238000006237 Beckmann rearrangement reaction Methods 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
229960002684 aminocaproic acid Drugs 0.000 description 1
235000011114 ammonium hydroxide Nutrition 0.000 description 1
239000012223 aqueous fraction Substances 0.000 description 1
238000000998 batch distillation Methods 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
238000004364 calculation method Methods 0.000 description 1
239000003990 capacitor Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000002131 composite material Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000002826 coolant Substances 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
238000011049 filling Methods 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
150000002443 hydroxylamines Chemical class 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
238000009413 insulation Methods 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
SQDFHQJTAWCFIB-UHFFFAOYSA-N n-methylidenehydroxylamine Chemical compound ON=C SQDFHQJTAWCFIB-UHFFFAOYSA-N 0.000 description 1
208000002761 neurofibromatosis 2 Diseases 0.000 description 1
125000002560 nitrile group Chemical group 0.000 description 1
239000011368 organic material Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
150000002923 oximes Chemical class 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
238000012545 processing Methods 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
230000009467 reduction Effects 0.000 description 1
238000007670 refining Methods 0.000 description 1
239000010802 sludge Substances 0.000 description 1
239000002002 slurry Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
239000006200 vaporizer Substances 0.000 description 1
239000002699 waste material Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D201/00—Preparation, separation, purification or stabilisation of unsubstituted lactams
- C07D201/02—Preparation of lactams
- C07D201/08—Preparation of lactams from carboxylic acids or derivatives thereof, e.g. hydroxy carboxylic acids, lactones or nitriles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/02—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D223/06—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D223/08—Oxygen atoms
- C07D223/10—Oxygen atoms attached in position 2

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Other In-Based Heterocyclic Compounds (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

SK5107-2007A 2005-03-18 2006-03-15 Zlepšený spôsob prípravy kaprolaktámu z nečisteného 6-aminokapronitrilu SK51072007A3 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US11/083,715 US7390897B2 (en)	2005-03-18	2005-03-18	Method for making caprolactam from impure 6-aminocapronitrile
PCT/US2006/009231 WO2006101870A1 (en)	2005-03-18	2006-03-15	Improved method for making caprolactam from impure 6-aminocapronitrile

Publications (1)

Publication Number	Publication Date
SK51072007A3 true SK51072007A3 (sk)	2008-12-05

Family

ID=36658684

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK5107-2007A SK51072007A3 (sk)	2005-03-18	2006-03-15	Zlepšený spôsob prípravy kaprolaktámu z nečisteného 6-aminokapronitrilu

Country Status (13)

Country	Link
US (1)	US7390897B2 (cs)
EP (1)	EP1858842A1 (cs)
JP (1)	JP5101486B2 (cs)
KR (1)	KR101273828B1 (cs)
CN (1)	CN101142178B (cs)
BR (1)	BRPI0609845A2 (cs)
CA (1)	CA2600769A1 (cs)
CZ (1)	CZ2007623A3 (cs)
MX (1)	MX2007011229A (cs)
MY (1)	MY140069A (cs)
SK (1)	SK51072007A3 (cs)
TW (1)	TW200700382A (cs)
WO (1)	WO2006101870A1 (cs)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN104557705B (zh) *	2013-10-15	2017-06-09	中国石油化工股份有限公司	一种己内酰胺精制的方法和装置

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2357484A (en)	1941-09-12	1944-09-05	Du Pont	Process for producing compounds containing an n-substituted amide group
US2301964A (en)	1941-09-12	1942-11-17	Du Pont	Method of preparing lactams
DE19500041A1 (de) *	1995-01-03	1996-07-04	Basf Ag	Verfahren zur kontinuierlichen Reinigung von aus 6-Aminocapronitril hergestelltem Roh-Caprolactam
FR2751962B1 (fr) *	1996-08-02	1998-09-11	Rhone Poulenc Fibres	Procede de purification de lactames
DE19753301A1 (de) *	1997-12-01	1999-06-02	Basf Ag	Verfahren zur Herstellung von Lactamen
US6716977B1 (en) *	2003-06-17	2004-04-06	E. I. Du Pont De Nemours And Company	Method for making caprolactam from impure ACN wherein ammonia and water are removed from crude caprolactam in a simple separation step and then THA is removed from the resulting caprolactam melt

2005
- 2005-03-18 US US11/083,715 patent/US7390897B2/en not_active Expired - Fee Related
2006
- 2006-03-15 SK SK5107-2007A patent/SK51072007A3/sk unknown
- 2006-03-15 KR KR1020077021277A patent/KR101273828B1/ko not_active Expired - Fee Related
- 2006-03-15 CZ CZ20070623A patent/CZ2007623A3/cs unknown
- 2006-03-15 CN CN2006800087210A patent/CN101142178B/zh not_active Expired - Lifetime
- 2006-03-15 EP EP06738305A patent/EP1858842A1/en not_active Withdrawn
- 2006-03-15 WO PCT/US2006/009231 patent/WO2006101870A1/en not_active Ceased
- 2006-03-15 BR BRPI0609845-2A patent/BRPI0609845A2/pt not_active Application Discontinuation
- 2006-03-15 CA CA002600769A patent/CA2600769A1/en not_active Abandoned
- 2006-03-15 JP JP2008501985A patent/JP5101486B2/ja not_active Expired - Fee Related
- 2006-03-15 MX MX2007011229A patent/MX2007011229A/es not_active Application Discontinuation
- 2006-03-17 TW TW095109266A patent/TW200700382A/zh unknown
- 2006-03-17 MY MYPI20061187A patent/MY140069A/en unknown

Also Published As

Publication number	Publication date
WO2006101870A1 (en)	2006-09-28
JP2008533159A (ja)	2008-08-21
CN101142178A (zh)	2008-03-12
MY140069A (en)	2009-11-30
US20080009618A9 (en)	2008-01-10
BRPI0609845A2 (pt)	2010-05-04
CN101142178B (zh)	2011-10-05
US20060211859A1 (en)	2006-09-21
EP1858842A1 (en)	2007-11-28
JP5101486B2 (ja)	2012-12-19
KR20080016529A (ko)	2008-02-21
TW200700382A (en)	2007-01-01
KR101273828B1 (ko)	2013-06-11
MX2007011229A (es)	2007-10-17
CA2600769A1 (en)	2006-09-28
CZ2007623A3 (cs)	2008-08-13
US7390897B2 (en)	2008-06-24

Legal Events

Date	Code	Title	Description
2013-01-02	FB9A	Suspension of patent application procedure

Publication	Publication Date	Title
KR100516986B1 (ko)	2005-09-26	6-아미노카프론산 유도체를 과열 수증기와 접촉시킴으로써 촉매 없이 카프로락탐을 제조하는 방법
US7060820B1 (en)	2006-06-13	Process for making caprolactam
KR20000052696A (ko)	2000-08-25	락탐 처리 방법
SK51072007A3 (sk)	2008-12-05	Zlepšený spôsob prípravy kaprolaktámu z nečisteného 6-aminokapronitrilu
US20050148803A1 (en)	2005-07-07	Method for the production of cyclohexanol from benzole
JP4961208B2 (ja)	2012-06-27	カプロラクタムの製造方法
KR20000070890A (ko)	2000-11-25	6-아미노카프로산 니트릴 및 이민을 함유하는 혼합물로부터 6-아미노카프로산 니트릴의 분리 방법
US7915403B2 (en)	2011-03-29	Production of lactams
JP2008533160A5 (cs)	2009-04-02
JP4961209B2 (ja)	2012-06-27	テトラヒドロアゼピンを含む不純な６−アミノカプロニトリルからカプロラクタムを製造する方法
KR20000070833A (ko)	2000-11-25	6-아미노카프로니트릴 및 이민을 함유하는 혼합물로부터6-아미노카프로니트릴의 분리 방법
JP4226083B2 (ja)	2009-02-18	ε−カプロラクタムの製造方法
KR20000004942A (ko)	2000-01-25	아민화 방법