SU860694A1 - Способ получени N-алкилкарбаматов - Google Patents

Способ получени N-алкилкарбаматов Download PDF

Info

Publication number: SU860694A1
Authority: SU; USSR - Soviet Union
Prior art keywords: general formula; alkyl; substituted; reaction; defined above
Prior art date: 1977-01-21

Application number

SU782566402A

Other languages

English (en)

Russian (ru)

Inventor

Райтель Кристиан

Кениг Карл-Гейнц

Мангольд Дитрих

Original Assignee

Басф Аг (Фирма)

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.)

1977-01-21

Filing date

1978-01-16

Publication date

1981-08-30

1978-01-16 Application filed by Басф Аг (Фирма) filed Critical Басф Аг (Фирма)

1981-08-30 Application granted granted Critical

1981-08-30 Publication of SU860694A1 publication Critical patent/SU860694A1/ru

Links

238000000034 method Methods 0.000 title claims abstract description 12
125000000217 alkyl group Chemical group 0.000 claims abstract description 4
-1 hydroxyl compound Chemical class 0.000 claims description 4
230000003993 interaction Effects 0.000 claims description 3
CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims description 2
125000001624 naphthyl group Chemical group 0.000 claims description 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
230000035484 reaction time Effects 0.000 claims description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract description 2
229910000041 hydrogen chloride Inorganic materials 0.000 abstract description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract description 2
238000004519 manufacturing process Methods 0.000 abstract description 2
239000002904 solvent Substances 0.000 abstract description 2
125000003118 aryl group Chemical group 0.000 abstract 1
125000004432 carbon atom Chemical group C* 0.000 abstract 1
239000007788 liquid Substances 0.000 abstract 1
238000002844 melting Methods 0.000 abstract 1
230000008018 melting Effects 0.000 abstract 1
239000000155 melt Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
HUNDISMVCBSIKO-UHFFFAOYSA-N (3,5-diethylphenyl) n-methylcarbamate Chemical compound CCC1=CC(CC)=CC(OC(=O)NC)=C1 HUNDISMVCBSIKO-UHFFFAOYSA-N 0.000 description 2
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
CRBJBYGJVIBWIY-UHFFFAOYSA-N 2-isopropylphenol Chemical compound CC(C)C1=CC=CC=C1O CRBJBYGJVIBWIY-UHFFFAOYSA-N 0.000 description 2
LPCJHUPMQKSPDC-UHFFFAOYSA-N 3,5-diethylphenol Chemical compound CCC1=CC(O)=CC(CC)=C1 LPCJHUPMQKSPDC-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
GRRYSIXDUIAUGY-UHFFFAOYSA-N n-methylcarbamoyl chloride Chemical compound CNC(Cl)=O GRRYSIXDUIAUGY-UHFFFAOYSA-N 0.000 description 2
238000004821 distillation Methods 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
238000002955 isolation Methods 0.000 description 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
238000003756 stirring Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

SU782566402A 1977-01-21 1978-01-16 Способ получени N-алкилкарбаматов SU860694A1 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19772702372 DE2702372A1 (de)	1977-01-21	1977-01-21	Verfahren zur herstellung von n-alkylcarbamaten

Publications (1)

Publication Number	Publication Date
SU860694A1 true SU860694A1 (ru)	1981-08-30

Family

ID=5999198

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU782566402A SU860694A1 (ru)	1977-01-21	1978-01-16	Способ получени N-алкилкарбаматов

Country Status (13)

Country	Link
JP (1)	JPS5392714A (fr)
BE (1)	BE863017A (fr)
CA (1)	CA1097676A (fr)
DD (1)	DD133793A5 (fr)
DE (1)	DE2702372A1 (fr)
FR (1)	FR2378002A1 (fr)
GB (1)	GB1594422A (fr)
HU (1)	HU175440B (fr)
IL (1)	IL53600A0 (fr)
IT (1)	IT1103262B (fr)
NL (1)	NL7800740A (fr)
SU (1)	SU860694A1 (fr)
ZA (1)	ZA78364B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6015771A (en) *	1998-05-22	2000-01-18	Bayer Aktiengesellschaft	Thermally-responsive record material
US6294502B1 (en)	1998-05-22	2001-09-25	Bayer Aktiengesellschaft	Thermally-responsive record material

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB191325971A (en) *	1913-11-12	1914-03-05	Bruno Beckmann Chem Fab G M B	Improved Manufacture of Carbamic Acid Ester of alpha-dichlorhydrin.
CH383945A (de) *	1960-04-14	1964-11-15	Geigy Ag J R	Verfahren zur Herstellung von neuen Arylcarbamaten und deren Verwendung zur Insektenbekämpfung
GB1054673A (fr) *	1962-08-23
GB1042203A (en) *	1963-04-09	1966-09-14	Robert J Geary	Substituted phenyl carbamates and their use as plant growth regulants

1977
- 1977-01-21 DE DE19772702372 patent/DE2702372A1/de not_active Withdrawn
- 1977-12-13 IL IL53600A patent/IL53600A0/xx unknown
- 1977-12-16 CA CA293,294A patent/CA1097676A/fr not_active Expired
1978
- 1978-01-09 JP JP60578A patent/JPS5392714A/ja active Pending
- 1978-01-16 SU SU782566402A patent/SU860694A1/ru active
- 1978-01-18 BE BE184400A patent/BE863017A/fr unknown
- 1978-01-18 IT IT47692/78A patent/IT1103262B/it active
- 1978-01-19 DD DD7800203306A patent/DD133793A5/xx unknown
- 1978-01-20 HU HU78BA3617A patent/HU175440B/hu unknown
- 1978-01-20 NL NL7800740A patent/NL7800740A/xx not_active Application Discontinuation
- 1978-01-20 ZA ZA00780364A patent/ZA78364B/xx unknown
- 1978-01-20 GB GB2348/78A patent/GB1594422A/en not_active Expired
- 1978-01-20 FR FR7801658A patent/FR2378002A1/fr not_active Withdrawn

Also Published As

Publication number	Publication date
CA1097676A (fr)	1981-03-17
IL53600A0 (en)	1978-03-10
BE863017A (fr)	1978-07-18
IT7847692A0 (it)	1978-01-18
DD133793A5 (de)	1979-01-24
HU175440B (hu)	1980-08-28
FR2378002A1 (fr)	1978-08-18
JPS5392714A (en)	1978-08-15
NL7800740A (nl)	1978-07-25
IT1103262B (it)	1985-10-14
DE2702372A1 (de)	1978-07-27
GB1594422A (en)	1981-07-30
ZA78364B (en)	1979-01-31

Similar Documents

Publication	Publication Date	Title
EP0046626B1 (fr)	1984-02-08	Isocyanates de benzènesulfonyl substitués et leur préparation
KR910007893A (ko)	1991-05-30	설포닐아미노 카보닐트리아졸리논
SU860694A1 (ru)	1981-08-30	Способ получени N-алкилкарбаматов
NO764110L (fr)	1977-06-06
DE68902001D1 (de)	1992-08-13	Verfahren zur herstellung von s-metoprolol und dessen zwischenprodukten.
EP0101023A1 (fr)	1984-02-22	Procédé de préparation de dérivés de 2-carbamoyloxyalkyl-1,4-dihydropyridines et intermédiaires utiles dans la préparation
US2437388A (en)	1948-03-09	Z-oxazolidone compounds and proc
CA1068717A (fr)	1979-12-25	Procede pour la preparation de derives carbamate et uree
US4629491A (en)	1986-12-16	Oxidized sulfur derivatives of diaminophosphinyl compounds as urease inhibitors and urease inhibited urea based fertilizer compositions
US5698729A (en)	1997-12-16	Process for preparing 6-alkoxy-(6H)-dibenzo C,E! 1,2!-oxaphosphorines
HUT36799A (en)	1985-10-28	Process for producing cepheme-carboxylic acid derivatives and pharmaceutical compositions containing them
IE41158B1 (en)	1979-10-24	Thiophosphoric acid esters having pesticidal properties
US3100790A (en)	1963-08-13	Isocyanoaryl esters of phosphonic, phosphinic, thiophosphonic, and thiophosphinic acids
JPS603317B2 (ja)	1985-01-26	塩化ホスフアイトの製造方法
CA1292479C (fr)	1991-11-26	Procede pour la fabrication de n-(sulfonylmethyl)formamides
US4000172A (en)	1976-12-28	Thio-derivatives of vanadium and processes for their preparation
GB1490797A (en)	1977-11-02	Oxa-or thia-diaza compounds and their fungicidal use
US4617387A (en)	1986-10-14	Bismorpholines and a process for their preparation
IE43468B1 (en)	1981-03-11	Production of thiocarbamic acid esters
EP0079991B1 (fr)	1986-02-26	Procédé de préparation de thiobiscarbamates
GB1457235A (en)	1976-12-01	N-dithiophosphoryl-carbamic acid esters and their use as insecticides and acaricides
CA1110385A (fr)	1981-10-06	Esters polymeres actives de 3,4-di-hydroxy-2,5- diphenyl-thiophene-1,1-di-oxyde
US4339382A (en)	1982-07-13	Process for manufacturing N-arylthiocarbamoyl-2-amino-1H-isoindole-1,3-(2H)diones
JP3851990B2 (ja)	2006-11-29	アクリロイルカルバメートの製造方法
US4150034A (en)	1979-04-17	Process for the preparation of substituted-phenyl-N-alkyl-carbamates