HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236047Generated: October 30, 2026
Benzoyl chloride → S-tert-Butyl benzenecarbothioate
https://huagongshe.com/reaction/2236047
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 86594189 | HCID 86594189 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | S-tert-Butyl benzenecarbothioate | HCID 12492106 | 50.1% |
Reaction Steps
S-t-butyl thiobenzoate t-Butyl mercaptan (6.15 g, 0.068 mol) was added dropwise to a solution of benzoyl chloride (10.5 g, 0.075 mol) in pyridine (6 g). The resulting mixture was allowed to stir for two hours at room temperature then poured onto ice-water and the mixture extracted with diethyl ether. The organic extract was washed with dilute HCl, water and brine and finally dried over anhydrous sodium sulfate. After removal of solvent and vacuum distillation, S-t-butyl thiobenzoate was obtained (6.64 g, 50.1% yield), b.p. 86° C. (0.8 mmHg). 1H-nmr (CDCl3) d (ppm): 1.60 (s, 9H, 3×CH3), 7.41 (m, 2H, ArH), 7.54 (m, 1H, ArH) and 7.94 (d, 2H, ArH). 13C-nmr (CDCl3) d (ppm): 29.8, 48.0, 126.8, 128.3, 132.7, 138.6 and 192.9. ii) t-Butyl Dithiobenzoate
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714075B1 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-da8bbb38f5a8496484dd9d37530c91b9 |
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| Source note | uspto-grants-2010_05 |
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