HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2,2-Difluoroethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2,2-Difluoroethan-1-ol | HCID 136187 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2-Difluoroethyl methanesulfonate | HCID 56776492 | 92% |
Reaction Steps
To a solution of 2,2-difluoro-ethanol (6 g, 73.12 mmol) and mesyl chloride (6.26 ml, 80.43 mmol) in CH2Cl2 (40 ml) was added triethylamine (12.66 ml, 87.74 mmol) dropwise at 0° C. After the addition was completed, the mixture was allowed to warm to room temperature and was stirred for 1 h. The reaction mixture was then washed two times with water and with brine and dried with Na2SO4. Evaporation of the solvent yielded the title compound (10.7 g, 92%) as yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592426B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-0eb96a49ce89424b8ad649c878ae4588 |
| Source note | uspto-grants-2013_11 |