GB1077031A - A process for the production of isocyanates - Google Patents
A process for the production of isocyanatesInfo
- Publication number
- GB1077031A GB1077031A GB127566A GB127566A GB1077031A GB 1077031 A GB1077031 A GB 1077031A GB 127566 A GB127566 A GB 127566A GB 127566 A GB127566 A GB 127566A GB 1077031 A GB1077031 A GB 1077031A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diisocyanate
- bis
- reaction
- isocyanates
- dimethyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C263/00—Preparation of derivatives of isocyanic acid
- C07C263/10—Preparation of derivatives of isocyanic acid by reaction of amines with carbonyl halides, e.g. with phosgene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/14—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides
- C07C319/20—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides by reactions not involving the formation of sulfide groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Isocyanates are prepared by reacting a primary amine, or an acid addition salt thereof, with at least a stoichiometric quantity of phosgene in the presence of a quantity of a tertiary amine sufficient to combine with the HCl formed during the reaction, and with any other acid which may be liberated. A large number of mono- and poly-amines are specified as starting materials. N,N-Dimethyl- and N,N-diethyl aniline are preferred tertiary amines. The reaction is usually effected at -10 DEG to 30 DEG C., but temperatures as high as 150 DEG C. may be employed. Examples relate to the preparation of bis-(4-isocyanatophenyl)-dimethyl methane, p-phenylene diisocyanate, cyclohexylisocyanate, ethyl isocyanate, hexamethylene diisocyanate, 1,4-butylene-bis-isocyanato-isopropyl ether, p-chlorophenylisocyanate, naphthalene - 2,7 - di - isocyanate, isopropylidene - 2,4,41 - triisocyanato - dibenzene and diphenylsulphide-4,41-diisocyanate.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF45410A DE1233854B (en) | 1965-03-03 | 1965-03-03 | Process for producing isocyanates |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1077031A true GB1077031A (en) | 1967-07-26 |
Family
ID=7100482
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB127566A Expired GB1077031A (en) | 1965-03-03 | 1966-01-11 | A process for the production of isocyanates |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1233854B (en) |
GB (1) | GB1077031A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7504533B2 (en) | 2006-04-24 | 2009-03-17 | Bayer Materialscience Llc | Process for the production of isocyanates |
US7547801B2 (en) | 2006-06-26 | 2009-06-16 | Bayer Materialscience Llc | Process for the continuous preparation of isocyanates |
US7645900B2 (en) | 2008-02-19 | 2010-01-12 | Bayer Materialscience Ag | Process for the preparation of isocyanates |
CN102659631A (en) * | 2011-12-24 | 2012-09-12 | 德州绿邦化工有限公司 | One-step synthesis of ethyl isocyanate |
CN107787317A (en) * | 2015-06-29 | 2018-03-09 | 科思创德国股份有限公司 | The method that hydrogen chloride for chemical reaction is provided |
US10112892B2 (en) | 2015-06-29 | 2018-10-30 | Covestro Deutschland Ag | Process for preparing polyisocyanates |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19833007A1 (en) * | 1998-07-23 | 2000-02-03 | Hoechst Schering Agrevo Gmbh | Process for the preparation of 4,6-disubstituted 2-isocyanatopyrimidines and their use as intermediates for drug synthesis |
DE10260082A1 (en) | 2002-12-19 | 2004-07-01 | Basf Ag | Process for the continuous production of isocyanates |
DE10260084A1 (en) | 2002-12-19 | 2004-07-01 | Basf Ag | Separation of a mixture of hydrogen chloride and phosgene |
-
1965
- 1965-03-03 DE DEF45410A patent/DE1233854B/en active Pending
-
1966
- 1966-01-11 GB GB127566A patent/GB1077031A/en not_active Expired
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7504533B2 (en) | 2006-04-24 | 2009-03-17 | Bayer Materialscience Llc | Process for the production of isocyanates |
US7547801B2 (en) | 2006-06-26 | 2009-06-16 | Bayer Materialscience Llc | Process for the continuous preparation of isocyanates |
US7645900B2 (en) | 2008-02-19 | 2010-01-12 | Bayer Materialscience Ag | Process for the preparation of isocyanates |
CN102659631A (en) * | 2011-12-24 | 2012-09-12 | 德州绿邦化工有限公司 | One-step synthesis of ethyl isocyanate |
CN102659631B (en) * | 2011-12-24 | 2014-05-07 | 德州绿邦化工有限公司 | One-step synthesis of ethyl isocyanate |
CN107787317A (en) * | 2015-06-29 | 2018-03-09 | 科思创德国股份有限公司 | The method that hydrogen chloride for chemical reaction is provided |
US10112892B2 (en) | 2015-06-29 | 2018-10-30 | Covestro Deutschland Ag | Process for preparing polyisocyanates |
CN107787317B (en) * | 2015-06-29 | 2020-08-28 | 科思创德国股份有限公司 | Method for providing hydrogen chloride for chemical reactions |
US10815193B2 (en) | 2015-06-29 | 2020-10-27 | Covestro Deutschland Ag | Process for providing hydrogen chloride for chemical reactions |
Also Published As
Publication number | Publication date |
---|---|
DE1233854B (en) | 1967-02-09 |
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