ES479380A1 - Process of preparation of 2- mercaptobenzthiazole - Google Patents
Process of preparation of 2- mercaptobenzthiazoleInfo
- Publication number
- ES479380A1 ES479380A1 ES479380A ES479380A ES479380A1 ES 479380 A1 ES479380 A1 ES 479380A1 ES 479380 A ES479380 A ES 479380A ES 479380 A ES479380 A ES 479380A ES 479380 A1 ES479380 A1 ES 479380A1
- Authority
- ES
- Spain
- Prior art keywords
- molar ratio
- nitrosobenzene
- reacted
- nitrobenzene
- specified molar
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles 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 in position 2
- C07D277/70—Sulfur atoms
- C07D277/72—2-Mercaptobenzothiazole
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Abstract
A process for the preparation of 2- mercaptobenzthiazole which comprises reacting nitrobenzene or nitrosobenzene, hydrogen sulphide and carbon disulphide, the molar ratio of nitrobenzene or nitrosobenzene: hydrogen sulphide being from 1:3 to 1:6 or from 1:1.5 to 1:4, the molar ratio of nitrobenzene or nitrosobenzene: carbon disulphide being from 1:1 to 1:3 and the final reaction temperature being from 200 to 300 DEG C, is disclosed. Embodiments are disclosed wherein (a) nitrobenzene and H25 are reacted in a specified molar ratio under elevated temperature and pressure and the resulting reaction mixture is reacted with CS2 in a specified molar ratio at 200 to 300 DEG C (b) nitrosobenzene, H25 and C52 are reacted in a specified molar ratio at 200 to 300 DEG C and (c) nitrosobenzene and H25 are reacted in a specified molar ratio at 20 to 100 DEG C and the resulting reaction mixture is reacted with C52 in a specified molar ratio at 200 to 300 DEG C.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2816407A DE2816407C3 (en) | 1978-04-15 | 1978-04-15 | Process for the preparation of 2-mercaptobenzothiazole |
| DE19782816503 DE2816503C3 (en) | 1978-04-15 | 1978-04-15 | Process for the preparation of 2-mercaptobenzothiazole |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES479380A1 true ES479380A1 (en) | 1979-07-16 |
Family
ID=25774251
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES479380A Expired ES479380A1 (en) | 1978-04-15 | 1979-04-06 | Process of preparation of 2- mercaptobenzthiazole |
Country Status (13)
| Country | Link |
|---|---|
| JP (1) | JPS54138555A (en) |
| BR (1) | BR7902252A (en) |
| CS (1) | CS209920B2 (en) |
| DD (1) | DD142879A5 (en) |
| ES (1) | ES479380A1 (en) |
| FR (1) | FR2432514A1 (en) |
| GB (1) | GB2018774B (en) |
| HU (1) | HU179918B (en) |
| IT (1) | IT1117172B (en) |
| NL (1) | NL7902705A (en) |
| PL (1) | PL119658B1 (en) |
| RO (1) | RO77250A (en) |
| SU (1) | SU1005661A3 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997046544A1 (en) * | 1996-06-03 | 1997-12-11 | Akzo Nobel N.V. | Acid catalysed process for preparing 2-mercaptobenzothiazole and derivatives thereof |
| US6222041B1 (en) * | 2000-02-24 | 2001-04-24 | Uniroyal Chemical Company, Inc. | Method for the production of 2-mercaptobenzothiazole |
-
1979
- 1979-04-06 NL NL7902705A patent/NL7902705A/en not_active Application Discontinuation
- 1979-04-06 ES ES479380A patent/ES479380A1/en not_active Expired
- 1979-04-11 BR BR7902252A patent/BR7902252A/en unknown
- 1979-04-11 CS CS792479A patent/CS209920B2/en unknown
- 1979-04-11 IT IT48697/79A patent/IT1117172B/en active
- 1979-04-11 PL PL1979214829A patent/PL119658B1/en unknown
- 1979-04-12 FR FR7909358A patent/FR2432514A1/en active Granted
- 1979-04-12 GB GB7913139A patent/GB2018774B/en not_active Expired
- 1979-04-12 DD DD79212194A patent/DD142879A5/en unknown
- 1979-04-13 JP JP4441279A patent/JPS54138555A/en active Pending
- 1979-04-13 SU SU792753405A patent/SU1005661A3/en active
- 1979-04-13 HU HU79AO478A patent/HU179918B/en unknown
- 1979-04-13 RO RO7997222A patent/RO77250A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| SU1005661A3 (en) | 1983-03-15 |
| FR2432514B1 (en) | 1983-07-29 |
| GB2018774A (en) | 1979-10-24 |
| PL119658B1 (en) | 1982-01-30 |
| JPS54138555A (en) | 1979-10-27 |
| IT7948697A0 (en) | 1979-04-11 |
| DD142879A5 (en) | 1980-07-16 |
| HU179918B (en) | 1983-01-28 |
| BR7902252A (en) | 1979-12-04 |
| GB2018774B (en) | 1982-12-01 |
| PL214829A1 (en) | 1980-01-14 |
| RO77250A (en) | 1981-08-17 |
| FR2432514A1 (en) | 1980-02-29 |
| NL7902705A (en) | 1979-10-17 |
| CS209920B2 (en) | 1981-12-31 |
| IT1117172B (en) | 1986-02-17 |
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