HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165991Generated: November 4, 2026
Benzyl mercaptan → 2-(Benzylsulfanyl)-4-chloro-1,3-thiazole
https://huagongshe.com/reaction/2165991
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2,4-Dichlorothiazole | HCID 12333155 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Benzylsulfanyl)-4-chloro-1,3-thiazole | HCID 15077118 | 90.7% |
Reaction Steps
Benzylmercaptan (24.8 g) was added dropwise to a solution of 10.8 of sodium methoxide in 100 ml ethanol. After stirring 15 minutes, the ethanolic solution of sodium benzylmercaptide was added dropwise to a solution of 30.8 g 2,4-dichlorothiazole [prepared by the method of P. Reynaud et al., Bull. Soc. Chim. France, 1735 (1962)], resulting in a temperature increase of 28° to 48°. When the exotherm subsided, the suspension was refluxed 1 hour, then the solvent was evaporated. Cold water (300 ml) was added to the oily residue, and the aqueous mixture was extracted with methylene chloride. The organic solution was washed with water, followed by saturated brine, then dried over magnesium sulfate, filtered and the solvent evaporated to give 43.8 g of 4-chloro-2-phenylmethylthiothiazole as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04943312 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-486820994f1c469ca0b5de720c35398e |
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| Source note | uspto-grants-1990_07 |
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