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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200638Generated: October 25, 2026

Methanesulfonyl chloride → 3,3,3-Trifluoropropyl methanesulfonate

https://huagongshe.com/reaction/2200638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3,3,3-Trifluoro-1-propanolHCID 137512—
SolventDichloromethaneHCID 6344—
Product3,3,3-Trifluoropropyl methanesulfonateHCID 2521050158.2%

Reaction Steps

To a solution of 3,3,3-trifluoropropan-1-ol (500 mg, 4.38 mmol) in DCM (10 mL) was added TEA (1.22 mL, 8.77 mmol) followed by dropwise addition of methanesulfonyl chloride (0.51 mL, 6.58 mmol) at 0° C. The resulting mixture was stirred at room temperature for 2 h. The reaction was diluted with DCM and the organic phase washed with brine, dried and concentrated to give crude product which was purified via silica gel chromatography eluting with petroleum ether/ethyl acetate (5:1) to give 3,3,3-trifluoropropyl methanesulfonate (490 mg, 58.2% yield) as light yellow oil. TLC (petroleum ether/ethyl acetate=3:1), Rf=0.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359359B2
Source datasetuspto-grants-2016_06
ORD IDord-a1aed81d00694da09b02c99e85dac7fa
Source noteuspto-grants-2016_06