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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279691Generated: October 26, 2026

Trichloroacetic Acid → 2,2,3,3,4,4,5,5,6,6-Decafluoro-1-(trichloromethyl)-1-cyclohexanol

https://huagongshe.com/reaction/279691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetic AcidHCID 6421—
ReactantDecafluorocyclohexanoneHCID 12570757—
SolventHexamethylphosphoramideHCID 12679—
Product2,2,3,3,4,4,5,5,6,6-Decafluoro-1-(trichloromethyl)-1-cyclohexanolHCID 22625236—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A solution of 30 g of perfluorocyclohexanone and 31.7 g of trichloroacetic acid was stirred in a pre-dried reaction vessel containing 113 mL of hexamethylphosphoramide. This mixture was cooled to −10° C. in a dry ice/acetone bath. Slight gas evolution was noted before and during the ketone addition. The stirred milky white reaction mixture was maintained at about 0° C. for an hour and then allowed to warm to 23° C. and stirring was continued 17 hours. The clear yellow solution was quenched with 150 mL of 10% HCl and then transferred to a separatory funnel with 400 mL of ethyl ether. This organic phase was washed with 4×500 mL of dilute HCl and then 300 mL of saturated NaCl solution. The solvent was removed by evaporation. The residue (33.7 g) contained 40.8% product by GC, confirmed by fluorine NMR. This carbinol can be converted to the corresponding acrylate by methods previously described (cf. Example 24).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362379B1
Source datasetuspto-grants-2002_03
ORD IDord-7b3b7fbfc0ea45f18e1526752e771514
Source noteuspto-grants-2002_03