HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(4-Bromo-2-(trifluoromethyl)phenoxy)ethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-(4-Bromo-2-(trifluoromethyl)phenoxy)-ethanol | HCID 57657583 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Bromo-2-(trifluoromethyl)phenoxy)ethyl methanesulfonate | HCID 86673356 | — |
Reaction Steps
2-(4-Bromo-2-(trifluoromethyl)phenoxy)ethanol (17.54 mmol, 5 g) and triethylamine (35.1 mmol, 4.88 ml, 3.55 g) were combined and stirred in DCM (100 ml) at 0° C. methanesulfonyl chloride (26.3 mmol, 2.036 ml, 3.01 g) was added and the reaction allowed to warm to room temperature over 1 hour. The reaction mixture was washed with water, dried over sodium sulfate and concentrated in vacuo to afford 2-(4-bromo-2-(trifluoromethyl)phenoxy)ethyl methanesulfonate. (5.64 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115126B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-a0419f61afaf428695f8db8a1aafd497 |
| Source note | uspto-grants-2015_08 |