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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113238Generated: October 30, 2026

Tetrahydrofuran → 1,1,1-Trifluoro-2-(trifluoromethyl)but-3-en-2-ol

https://huagongshe.com/reaction/2113238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHexafluoroacetoneHCID 12695—
ReactantHCID 178461836HCID 178461836—
Product1,1,1-Trifluoro-2-(trifluoromethyl)but-3-en-2-olHCID 3787958—

Reaction Steps

To 1.6 M vinylmagnesium chloride in THF (200 mL, 0.32 mol) at −78° C. was added hexafluoroacetone (50 g, 0.31 mol) by cannula over a period of 3 h with stirring. The reaction mixture was allowed to warm to r.t. and stirred for an additional 2 h, then heated to 40° C. for an additional 1 h. The reaction mixture was quenched with aqueous NH4Cl solution. The mixture was diluted with pentane, filtered, and the organic phase was dried over MgSO4. Fractional distillation (12 inch Vigreux column) at 100-103° C. afforded the product 1,1,1-trifluoro-2-trifluoromethyl-but-3-en-2-ol (mixture containing around 66 mol % THF) as a clear liquid (50 g). 1H NMR δ 5.20 (br, 1H), 5.70 (d, 1H), 5.92 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524969B2
Source datasetuspto-grants-2009_04
ORD IDord-094f7ce9c54f407596d3c79aadd08883
Source noteuspto-grants-2009_04