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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668268Generated: October 31, 2026

2,2,3,3-Tetrafluoro-1-propanol → 2,2,3,3-Tetrafluoropropyl trifluoromethanesulfonate

https://huagongshe.com/reaction/1668268

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,3,3-Tetrafluoro-1-propanolHCID 6441—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl fluoride, trifluoro-HCID 67631—
SolventChloroformHCID 6212—
Product2,2,3,3-Tetrafluoropropyl trifluoromethanesulfonateHCID 3792475—

Reaction Steps

2,2,3,3-tetrafluoropropan-1-ol (244.3 g, 1.85 mol, obtained from Sinochem Corp.), triethylamine (187.2 g, 1.85 mol, obtained from Aldrich Chemical Co.) and 500 mL of chloroform were combined in a 2-liter Parr pressure reactor and sealed. The reactor temperature was set to −10° C. Trifluoromethanesulfonyl fluoride (281.33 g, 1.85 mol, obtained from 3M Company) was added at such a rate that the temperature did not exceed −5° C. Once the addition was complete, the mix was held at −10° C. for 45 minutes. The reaction mix was then emptied and washed with 2×500 mL portions of water and 1×250 mL portion of 1N HCl. GC analysis of the reaction mixture indicated a 97 percent conversion to the product. The chloroform solvent was removed by rotary evaporation. The product was dried over anhydrous magnesium sulfate which was then filtered from the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07988877B2
Source datasetuspto-grants-2011_08
ORD IDord-4f99390ce87f463fb161039acb11fac7
Source noteuspto-grants-2011_08