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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385308Generated: October 30, 2026

Triethylamine → 4,4,4-Trifluorobutyl methanesulfonate

https://huagongshe.com/reaction/1385308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4,4,4-Trifluorobutan-1-olHCID 136307—
SolventDichloromethaneHCID 6344—
Product4,4,4-Trifluorobutyl methanesulfonateHCID 22725681988%

Reaction Steps

A stirred solution of 4,4,4-trifluorobutanol (35 g; 0.027 mol) and triethylamine (28.3 g; 0.280 mol) in 200 ml of dichloromethane was treated dropwise at 0° C. with a solution of methanesulphonyl chloride (32.1 g; 0.280 mol) in 100 ml of dichloromethane. After the end of the addition, the mixture was stirred for a further 30 min, then poured onto ice and the phases were subsequently separated. The organic phase was dried over magnesium sulphate and concentrated under reduced pressure. 55 g of crude 4,4,4-trifluorobutyl methanesulphonate were obtained as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262112B1
Source datasetuspto-grants-2001_07
ORD IDord-d8f8b65e30d24eddbcc696f323a79f82
Source noteuspto-grants-2001_07