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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422322Generated: November 1, 2026

4-tert-Butylcyclohexanone → 4-tert-butyl-1,1-difluorocyclohexane

https://huagongshe.com/reaction/1422322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylcyclohexanoneHCID 7392—
ReactantBoron trifluoride etherateHCID 8000—
Reactant4-FluoroanisoleHCID 9987—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
SolventDichloromethaneHCID 6344—
Product4-tert-butyl-1,1-difluorocyclohexaneHCID 64049967%

Reaction Steps

A solution of 4-t-butylcyclohexanone (308 mg, 2.0 mmol) in CH2Cl2 (10.0 mL) was added to diethylaminosulfur trifluoride (483 mg, 3.0 mmol ) at room temperature under N2. BF3.OEt2 (100 mL) was added and the mixture was stirred for 6 h at room temperature. The mixture was washed with saturated NaHCO3, dried (Na2SO4), filtered and evaporated in vacuo. Proton and Fluorine NMR with 4-fluoroanisole (2 mmol) as internal standard showed that a 67% yield of 1,1-difluoro-4-t-butylcyclohexane was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080886
Source datasetuspto-grants-2000_06
ORD IDord-8efbf6a3f34f4b318ddd7620f0bc4972
Source noteuspto-grants-2000_06