HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Benzenemethanol,2-fluoro-,1-methansulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Fluorobenzylic alcohol | HCID 67969 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzenemethanol,2-fluoro-,1-methansulfonate | HCID 21964506 | — |
Reaction Steps
To a solution of 2-Fluorobenzyl alcohol (10 g, 79.28 mmol) in dry dichloromethane (200 ml) was added triethylamine (12.03 g, 118.9 mmol) under argon at room temperature. Methanesulfonyl chloride (10.71 g, 93.5 mmol) was added to the above reaction mixture of 0° C., and stirring was continued for another 3 hours. Water (100 ml) was added to the reaction mixture and the mixture was extracted twice with dichloromethane. The combined organic layers were washed with water and brine. The reaction mixture was dried over Na2SO4, filtered and concentrated to give the title compound as an yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06858602B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-d2f54d8cf369460c8e6217de1054e9b8 |
| Source note | uspto-grants-2005_02 |