HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847125Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 13788291, compound
https://huagongshe.com/reaction/847125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Chloro-2-picoline | HCID 87601 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13788291 | HCID 13788291 | 34.9% |
Reaction Steps
12.8 g of 2-chloro-6-methylpyridine, 18 g of anhydrous potassium carbonate and 100 ml of dimethylsulfoxide were mixed to obtain a suspension. This suspension was preliminarily heated to a temperature of from 120° to 130° C., and 10 ml of a dimethylsulfoxide solution of 18.6 g of benzyl mercaptan was dropwise added thereto over a period of about 30 minutes. Then, the mixture was reacted at 150° C. for about one hour. Thereafter, the reaction solution was cooled, then put into water and extracted with methylene chloride. The methylene chloride layer was dried over anhydrous sodium sulfate, and then methylene chloride was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 7.53 g of oily 2-benzylthio-6-methylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05139565 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-7cf81faceb6345c49daf92f796885506 |
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| Source note | uspto-grants-1992_08 |
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