HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Benzenemethanol,2-fluoro-,1-methansulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| 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 | 65% |
Reaction Steps
To a solution of 2-fluorobenzyl alcohol (4.40 g, 34.9 mmol) in dichloromethane (40 mL) was added methanesulfonyl chloride (3.24 mL, 41.9 mmol) and triethylamine (5.84 mL, 41.9 mmol) on an ice bath, the solution was warmed to room temperature and stirred overnight. The reaction solution was diluted with dichloromethane, washed with an aqueous solution of 5% sodium bicarbonate, then, dried over anhydrous magnesium sulfate, the solvent was evaporated, and the title compound (4.62 g, 65%) was obtained as a brown oil. This was used in the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932272B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-59be7823e0ab49d396c7f30f5448a5c8 |
| Source note | uspto-grants-2011_04 |