HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273852Generated: October 31, 2026
Triethylamine → 2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl Methanesulfonate
https://huagongshe.com/reaction/273852
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethanol | HCID 10776163 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl Methanesulfonate | HCID 10519307 | — |
Reaction Steps
To a solution of 2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethanol (210 mg) in methylene chloride (1 ml) were added triethylamine (186 μl) and methanesulfonyl chloride (83 μl) with stirring under ice cooling, and the mixture was reacted at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure. To the concentrate was added water, and the mixture was extracted with diethyl ether. The extract was washed with water, dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by medium pressure liquid column chromatography on silica gel using a mixture of hexane and ethyl acetate (2/1) as eluent to give 273 mg of 2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl methansulfonate melting at 40.5°-42.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05387603 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-68eaa92338f647288ba099d25bf70c98 |
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| Source note | uspto-grants-1995_02 |
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