DK175156B1 - Fremgangsmåde til kontinuert fremstilling af acetater - Google Patents

Fremgangsmåde til kontinuert fremstilling af acetater Download PDF

Info

Publication number: DK175156B1
Authority: DK; Denmark
Prior art keywords: column; acetate; alcohol; mixture; catalyst
Prior art date: 1987-02-23

Application number

DK198800904A

Other languages

Danish (da)

English (en)

Other versions

DK90488D0 (da

DK90488A (da

Inventor

Michel Canonge

Jean Claude Joly

Original Assignee

Bp Chem Int Ltd

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.)

1987-02-23

Filing date

1988-02-22

Publication date

2004-06-21

1988-02-22 Application filed by Bp Chem Int Ltd filed Critical Bp Chem Int Ltd

1988-02-22 Publication of DK90488D0 publication Critical patent/DK90488D0/da

1988-08-24 Publication of DK90488A publication Critical patent/DK90488A/da

2004-06-21 Application granted granted Critical

2004-06-21 Publication of DK175156B1 publication Critical patent/DK175156B1/da

Links

QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 title claims abstract description 48
238000000034 method Methods 0.000 title claims abstract description 44
238000002360 preparation method Methods 0.000 title claims abstract description 11
239000000203 mixture Substances 0.000 claims abstract description 89
239000003054 catalyst Substances 0.000 claims abstract description 77
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 62
238000004821 distillation Methods 0.000 claims abstract description 43
150000001242 acetic acid derivatives Chemical class 0.000 claims abstract description 16
238000005809 transesterification reaction Methods 0.000 claims abstract description 11
150000003333 secondary alcohols Chemical class 0.000 claims abstract description 10
239000007791 liquid phase Substances 0.000 claims abstract description 5
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 42
238000006243 chemical reaction Methods 0.000 claims description 16
125000004432 carbon atom Chemical group C* 0.000 claims description 10
230000003197 catalytic effect Effects 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 9
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 7
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 7
KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims description 7
229910052719 titanium Inorganic materials 0.000 claims description 7
239000010936 titanium Substances 0.000 claims description 7
ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 claims description 6
230000015572 biosynthetic process Effects 0.000 claims description 5
MGMXTRZFWPWZFH-UHFFFAOYSA-N 2-ethoxypropan-2-ol Chemical compound CCOC(C)(C)O MGMXTRZFWPWZFH-UHFFFAOYSA-N 0.000 claims description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 4
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
229910052751 metal Inorganic materials 0.000 claims description 3
239000002184 metal Substances 0.000 claims description 3
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 2
LOTBYPQQWICYBB-UHFFFAOYSA-N methyl n-hexyl-n-[2-(hexylamino)ethyl]carbamate Chemical compound CCCCCCNCCN(C(=O)OC)CCCCCC LOTBYPQQWICYBB-UHFFFAOYSA-N 0.000 claims description 2
230000000737 periodic effect Effects 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
239000003153 chemical reaction reagent Substances 0.000 abstract description 24
150000001298 alcohols Chemical class 0.000 abstract description 13
230000009257 reactivity Effects 0.000 abstract description 5
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 28
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 14
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
239000007788 liquid Substances 0.000 description 10
239000012429 reaction media Substances 0.000 description 10
239000000047 product Substances 0.000 description 8
LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 8
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 7
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
ZHFCYDPONPCVOH-UHFFFAOYSA-N 2-ethoxypropan-2-yl acetate Chemical compound CCOC(C)(C)OC(C)=O ZHFCYDPONPCVOH-UHFFFAOYSA-N 0.000 description 5
150000002170 ethers Chemical class 0.000 description 5
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
WFDIJRYMOXRFFG-UHFFFAOYSA-N acetic acid anhydride Natural products CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 4
239000006227 byproduct Substances 0.000 description 4
238000000926 separation method Methods 0.000 description 4
238000007086 side reaction Methods 0.000 description 4
238000000746 purification Methods 0.000 description 3
KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
238000010586 diagram Methods 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
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 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
125000003158 alcohol group Chemical group 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
NBZANZVJRKXVBH-GYDPHNCVSA-N alpha-Cryptoxanthin Natural products O[C@H]1CC(C)(C)C(/C=C/C(=C\C=C\C(=C/C=C/C=C(\C=C\C=C(/C=C/[C@H]2C(C)=CCCC2(C)C)\C)/C)\C)/C)=C(C)C1 NBZANZVJRKXVBH-GYDPHNCVSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
230000007547 defect Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000009776 industrial production Methods 0.000 description 1
239000003456 ion exchange resin Substances 0.000 description 1
229920003303 ion-exchange polymer Polymers 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
NMRPBPVERJPACX-UHFFFAOYSA-N octan-3-ol Chemical compound CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000012071 phase Substances 0.000 description 1
229920001521 polyalkylene glycol ether Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
125000000075 primary alcohol group Chemical group 0.000 description 1
150000003138 primary alcohols Chemical class 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000010517 secondary reaction Methods 0.000 description 1
238000001577 simple distillation Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/03—Preparation of carboxylic acid esters by reacting an ester group with a hydroxy group

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Ultra Sonic Daignosis Equipment (AREA)
Investigating Or Analyzing Materials By The Use Of Ultrasonic Waves (AREA)

DK198800904A 1987-02-23 1988-02-22 Fremgangsmåde til kontinuert fremstilling af acetater DK175156B1 (da)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR8702454A FR2611704B1 (fr)	1987-02-23	1987-02-23	Procede de fabrication en continu d'acetates
FR8702454		1987-02-23

Publications (3)

Publication Number	Publication Date
DK90488D0 DK90488D0 (da)	1988-02-22
DK90488A DK90488A (da)	1988-08-24
DK175156B1 true DK175156B1 (da)	2004-06-21

Family

ID=9348272

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DK198800904A DK175156B1 (da)	1987-02-23	1988-02-22	Fremgangsmåde til kontinuert fremstilling af acetater

Country Status (14)

Country	Link
US (1)	US4960927A (de)
EP (1)	EP0280471B1 (de)
JP (1)	JP2768681B2 (de)
AT (1)	ATE66670T1 (de)
AU (1)	AU611412B2 (de)
CA (1)	CA1305719C (de)
DE (1)	DE3864419D1 (de)
DK (1)	DK175156B1 (de)
ES (1)	ES2024016B3 (de)
FI (1)	FI89591C (de)
FR (1)	FR2611704B1 (de)
GR (1)	GR3002622T3 (de)
NO (1)	NO167973C (de)
PT (1)	PT86804B (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4344358A1 (de) *	1993-12-24	1995-06-29	Henkel Kgaa	Verfahren zum Aufarbeiten eines Reaktionsgemischs mittels einer auf den Reaktor aufgesetzen Kolonne
FR2757156B1 (fr) *	1996-12-17	1999-01-22	Bp Chemicals Snc	Procede de fabrication en continu d'esters
DE10044352A1 (de) *	2000-09-07	2002-03-21	Basf Ag	Kontinuierliches Verfahren zur Herstellung von Acetalen
WO2007063757A1 (ja) *	2005-11-30	2007-06-07	Asahi Kasei Chemicals Corporation	高品質芳香族ポリカーボネートの工業的製造方法
TW200738781A (en) *	2005-12-12	2007-10-16	Asahi Kasei Chemicals Corp	Process for industrially producing high-quality aromatic polycarbonate
KR100707831B1 (ko)	2005-12-22	2007-04-13	한국에너지기술연구원	노말 부틸아세테이트를 제조하는 방법 및 그 제조 장치

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB970431A (de) *	1961-02-04	1900-01-01
US3700726A (en) *	1971-02-19	1972-10-24	Eastman Kodak Co	Process for the manufacture of glycol ether acetates
US4260813A (en) *	1978-02-02	1981-04-07	Showa Denko K.K.	Process for the continuous production of ethylene glycol monoethyl ether acetate
DE3019767A1 (de) *	1980-05-23	1981-12-03	Basf Ag, 6700 Ludwigshafen	Verfahren zur kontinuierlichen herstellung von essigsaeureestern
JPS58183640A (ja) *	1982-04-20	1983-10-26	Nippon Synthetic Chem Ind Co Ltd:The	酢酸エステルの製造方法
CH660599A5 (de) *	1984-07-26	1987-05-15	Ciba Geigy Ag	Loesungen anionischer farbstoffe.

1987
- 1987-02-23 FR FR8702454A patent/FR2611704B1/fr not_active Expired
1988
- 1988-02-18 ES ES88301393T patent/ES2024016B3/es not_active Expired - Lifetime
- 1988-02-18 NO NO880720A patent/NO167973C/no not_active IP Right Cessation
- 1988-02-18 DE DE8888301393T patent/DE3864419D1/de not_active Expired - Lifetime
- 1988-02-18 EP EP88301393A patent/EP0280471B1/de not_active Expired - Lifetime
- 1988-02-18 AT AT88301393T patent/ATE66670T1/de not_active IP Right Cessation
- 1988-02-22 CA CA000559415A patent/CA1305719C/en not_active Expired - Lifetime
- 1988-02-22 DK DK198800904A patent/DK175156B1/da not_active IP Right Cessation
- 1988-02-22 AU AU12047/88A patent/AU611412B2/en not_active Expired
- 1988-02-22 PT PT86804A patent/PT86804B/pt not_active IP Right Cessation
- 1988-02-22 JP JP63037686A patent/JP2768681B2/ja not_active Expired - Lifetime
- 1988-02-23 FI FI880843A patent/FI89591C/fi active IP Right Grant
1989
- 1989-12-05 US US07/449,516 patent/US4960927A/en not_active Expired - Lifetime
1991
- 1991-08-29 GR GR91401197T patent/GR3002622T3/el unknown

Also Published As

Publication number	Publication date
CA1305719C (en)	1992-07-28
FI89591C (fi)	1993-10-25
AU1204788A (en)	1988-08-25
FI880843A0 (fi)	1988-02-23
GR3002622T3 (en)	1993-01-25
DK90488D0 (da)	1988-02-22
NO167973C (no)	1992-01-02
AU611412B2 (en)	1991-06-13
ES2024016B3 (es)	1992-02-16
FI880843A7 (fi)	1988-08-24
FR2611704B1 (fr)	1989-06-09
FI89591B (fi)	1993-07-15
PT86804B (pt)	1992-05-29
EP0280471B1 (de)	1991-08-28
EP0280471A1 (de)	1988-08-31
DK90488A (da)	1988-08-24
DE3864419D1 (de)	1991-10-02
NO880720L (no)	1988-08-24
ATE66670T1 (de)	1991-09-15
FR2611704A1 (fr)	1988-09-09
JP2768681B2 (ja)	1998-06-25
PT86804A (pt)	1988-03-01
US4960927A (en)	1990-10-02
NO880720D0 (no)	1988-02-18
NO167973B (no)	1991-09-23
JPS63246349A (ja)	1988-10-13

Legal Events

Date	Code	Title	Description
2008-03-10	PUP	Patent expired

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