HU180807B - Process for producing esters of alkyl-thio-chloro-formic acid - Google Patents
Process for producing esters of alkyl-thio-chloro-formic acid Download PDFInfo
- Publication number
- HU180807B HU180807B HUCE001165A HU180807B HU 180807 B HU180807 B HU 180807B HU CE001165 A HUCE001165 A HU CE001165A HU 180807 B HU180807 B HU 180807B
- Authority
- HU
- Hungary
- Prior art keywords
- phosgene
- stage
- mercaptan
- activated carbon
- unreacted
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 8
- 150000002148 esters Chemical class 0.000 title claims description 5
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims abstract description 41
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 26
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000011261 inert gas Substances 0.000 claims abstract description 9
- 239000003054 catalyst Substances 0.000 claims abstract description 8
- 238000010438 heat treatment Methods 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims description 8
- 239000012467 final product Substances 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 5
- 238000010924 continuous production Methods 0.000 claims description 3
- 239000007789 gas Substances 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims 2
- 238000007664 blowing Methods 0.000 claims 1
- -1 alkyl mercaptan Chemical compound 0.000 abstract 1
- WQAQPCDUOCURKW-UHFFFAOYSA-N butanethiol Chemical compound CCCCS WQAQPCDUOCURKW-UHFFFAOYSA-N 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 3
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- KTRFZWJCHOQHMN-UHFFFAOYSA-N chloromethanethioic s-acid Chemical compound SC(Cl)=O KTRFZWJCHOQHMN-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- VYMLCIOLHVSKHO-UHFFFAOYSA-N o-octyl octylsulfanylmethanethioate Chemical compound CCCCCCCCOC(=S)SCCCCCCCC VYMLCIOLHVSKHO-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C329/00—Thiocarbonic acids; Halides, esters or anhydrides thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772721683 DE2721683A1 (de) | 1977-05-13 | 1977-05-13 | Verfahren zur herstellung von alkylthiochlorameisensaeureestern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU180807B true HU180807B (en) | 1983-04-29 |
Family
ID=6008907
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HUCE001165 HU180807B (en) | 1977-05-13 | 1978-05-12 | Process for producing esters of alkyl-thio-chloro-formic acid |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE866856A (enrdf_load_stackoverflow) |
| DE (1) | DE2721683A1 (enrdf_load_stackoverflow) |
| HU (1) | HU180807B (enrdf_load_stackoverflow) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4012405A (en) * | 1975-11-28 | 1977-03-15 | Stauffer Chemical Company | Production of ethyl chlorothioformate |
-
1977
- 1977-05-13 DE DE19772721683 patent/DE2721683A1/de active Granted
-
1978
- 1978-05-09 BE BE187520A patent/BE866856A/xx not_active IP Right Cessation
- 1978-05-12 HU HUCE001165 patent/HU180807B/hu unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BE866856A (fr) | 1978-11-09 |
| DE2721683C2 (enrdf_load_stackoverflow) | 1987-10-29 |
| DE2721683A1 (de) | 1978-11-23 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HU90 | Patent valid on 900628 |