HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-(Methylsulfonyl)ethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(Methylsulfonyl)ethanol | HCID 84834 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Methylsulfonyl)ethyl methanesulfonate | HCID 18464597 | — |
Reaction Steps
Combine 2-methylsulfonylethanol (7.7 g, 62 mmol) and dichloromethane (50 mL). Cool in an ice bath. Add methanesulfonyl chloride (7.81 g , 68.2 mmol). Add diisopropylethylamine (8.0 g, 62 mmol). After the addition of diisopropylethylamine, warm to ambient temperature. After 12 hours, add water and separate the layers. Extract the organic layer with a saturated aqueous sodium bicarbonate solution. Dry the organic layer over Na2SO4, filter and evaporate in vacuo to give the title compound: mp; 55-57° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05932571 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-10eb86874aa74fcbabb9ba415c898f60 |
| Source note | uspto-grants-1999_08 |