HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073693Generated: October 31, 2026
Benzyl mercaptan → 4-(Benzylsulfanyl)-1,3-thiazole
https://huagongshe.com/reaction/2073693
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-Chloro-1,3-thiazole | HCID 13517394 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(Benzylsulfanyl)-1,3-thiazole | HCID 15077120 | 37.8% |
Reaction Steps
Benzylmercaptan (24.8 g) was added slowly to a solution of 10.8 g of sodium methoxide in 100 ml ethanol. After 10 minutes, the reaction mixture was heated to 65° C. and a solution of 23.8 g of 4-chlorothiazole [prepared by the method of P. Reynaud et al., Bull. Soc. Chim. France, 1735 (1962)] in 25 ml ethanol was added dropwise. When addition was complete, the reaction mixture was refluxed 36 hours. The reaction mixture was cooled, and the bulk of the solvent evaporated. Cold water (300 ml) was added to the residue, and the aqueous mixture was extracted with 200 ml ether followed by 200 ml methylene chloride. The combined organic solution was washed with brine, dried over magnesium sulfate, filtered and the solvent evaporated. Distillation of the resulting yellow oil gave 15.6 g of 4-(phenylmethylthio)thiazole, bp 122-134 (0.6 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04919706 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-bbed34baa8114ff89f3a5ec24279a3aa |
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| Source note | uspto-grants-1990_04 |
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