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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113242Generated: October 31, 2026

Hexafluoroacetone → 1,1,1-Trifluoro-2-trifluoromethyl-but-3-yn-2-ol

https://huagongshe.com/reaction/2113242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexafluoroacetoneHCID 12695—
ReactantHCID 178418486HCID 178418486—
Product1,1,1-Trifluoro-2-trifluoromethyl-but-3-yn-2-olHCID 13667828—

Reaction Steps

To a 100 ml solution of ethynyl magnesium bromide (0.5 M in THF) in an acetone-ethanol dry ice bath was bubbled hexafluoro acetone gas (6.1 g, 36.7 mmol) over 2 h. The reaction mixture was warmed to r.t and then refluxed for 0.5 h. The reaction mixture was quenched with aqueous NH4Cl solution and extracted with ether. The combined organic phases were washed with brine, and dried over MgSO4. A liquid mixture of 1,1,1-trifluoro-2-trifluoromethyl-but-3-yn-2-ol with THF at b.p. 100-103° C. (4.7 g, contained about 68 mol % THF) was obtained by distillation (12 inch Vigreux column).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524969B2
Source datasetuspto-grants-2009_04
ORD IDord-bc101de70dbe4fdab6d0c8d48c1a3cbf
Source noteuspto-grants-2009_04