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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643521Generated: November 1, 2026

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

https://huagongshe.com/reaction/1643521

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 numberUS08119819B2
Source datasetuspto-grants-2012_02
ORD IDord-bc0f9e64dc2c410f9952536a047ea73f
Source noteuspto-grants-2012_02