Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424319Generated: October 29, 2026

Ethyl ketone → 7,7,7-Trifluoro-3-ethyl-3-heptanol

https://huagongshe.com/reaction/424319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ketoneHCID 7288—
Reactant4-Bromo-1,1,1-trifluorobutaneHCID 521006—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product7,7,7-Trifluoro-3-ethyl-3-heptanolHCID 8664009276.1%

Reaction Steps

1.3 g of magnesium, 10.0 g of 1-bromo-4,4,4-trifluorobutane and 20 g of tetrahydrofuran were charged into a four-necked flask equipped with a nitrogen feeding tube, a reflux condenser, a dropping funnel and a thermometer, and a Grignard reagent was prepared by a conventional method. Then, a mixture of 5.0 g of 3-pentanone and 4 g of tetrahydrofuran was dropwise added to the obtained Grignard reagent at a temperature of 25 to 35° C. over 30 minutes, followed by stirring at the same temperature for 1 hour. The reaction mixture was treated by a conventional method, and the resulting organic phase was washed with water, followed by drying with anhydrous magnesium sulfate. Thereafter, the resultant was concentrated under reduced pressure, thereby obtaining 7.9 g of 7,7,7-trifluoro-3-ethyl-3-heptanol in the form of a pale yellow oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08105747B2
Source datasetuspto-grants-2012_01
ORD IDord-bdb25224107a4e85b544c56d315a6230
Source noteuspto-grants-2012_01