Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | CID 15930840 | HCID 15930840 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 178527790 | HCID 178527790 | — |
Reaction Steps
To a stirred solution of 4-chloroaniline (2.55 g) in acetic acid (5 cm3) was added sulphur monochloride (10 cm3) causing formation of a thick red slurry. The reaction was heated at 60° C. for 4 hours giving a mixture of green solid and a green solution. The mixture was diluted with hexane and the green solid was filtered off. The solid was taken into water and 2M NaOH was added and the mixture heated for 4 hours at 100° C. and then filtered through celite to give a pale pink filtrate. Carbon disulphide (2 cm3) was added to the filtrate and the reaction was heated at reflux for 15 hours. The mixture was cooled and acidlied to pH 1 causing formation of a thick yellow precipitate. Filtration and recrystallisation from ethanol/acetone/water gave 6-chloro-2-mercaptobenzthiazole as a white solid. 1H NMR (DMSO): d 7.97 (1H, d), 7.58 (1H, dd), 7.41 (1 H, d). Mp 251°-253° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05451594 |
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| Source dataset | uspto-grants-1995_09 |
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| ORD ID | ord-7af06c3180f842efb2af6d9c06484db4 |
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| Source note | uspto-grants-1995_09 |
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