HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-(2-Thienyl)ethyl methanesulphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Thiopheneethanol | HCID 79400 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-(2-Thienyl)ethyl methanesulphonate | HCID 3047723 | — |
Reaction Steps
A mixture of 12.8 g of 2-(2-thienyl)ethanol, 450 ml. of dichloromethane and 20.2 g. of triethylamine is chilled to -10° C. and 12.8 g. of cold methanesulfonyl chloride is added dropwise over 30 minutes. After stirring for 1 hour, the mixture is washed with 300 ml. of cold water, 300 ml. of cold 10% hydrochloric acid, 300 ml. of cold saturated sodium bicarbonate, and 300 ml. of cold saturated sodium chloride solution. The organic layer is dried over magnesium sulfate and concentrated under vacuum to give the product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04246275 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-3011350c92114428a5c2383781b86b62 |
| Source note | uspto-grants-1981_01 |