HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → Pyridine, 3-chloro-2-[(phenylmethyl)thio]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Dichloropyridine | HCID 16988 | — |
| Solvent | Water | HCID 962 | — |
| Product | Pyridine, 3-chloro-2-[(phenylmethyl)thio]- | HCID 19881832 | 78.5% |
Reaction Steps
10 g of 2,3-dichloropyridine, 11.2 g of anhydrous potassium carbonate and 100 ml of dimethylsulfoxide were mixed to obtain a suspension. To this suspension, 10 ml of a dimethylsulfoxide solution of 10.1 g of benzyl mercaptan was dropwise added over a period of about 20 minutes at 110° C. Then, the mixture was reacted at a temperature of from 120 to 130° C. for about 1.5 hours. Thereafter, the reaction product was put into water and extracted with methylene chloride. The methylene chloride layer was dried over anhydrous sodium sulfate. Then, methylene chloride was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography to obtain 12.5 g of oily 2-benzylthio-3-chloropyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05139565 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-6682ecc6a224494b8df2baba399919ba |
| Source note | uspto-grants-1992_08 |