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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595996Generated: October 27, 2026

1,3,5-Trichloro-2,4,6-trifluorobenzene → 1-(3,5-Dichloro-2,4,6-trifluorophenyl)perfluorocyclohexanol

https://huagongshe.com/reaction/1595996

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,5-Trichloro-2,4,6-trifluorobenzeneHCID 67573—
ReactantDecafluorocyclohexanoneHCID 12570757—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product1-(3,5-Dichloro-2,4,6-trifluorophenyl)perfluorocyclohexanolHCID 2262527362.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under a N2 atmosphere 29.5 g of 1,3,5-trichloro-2,4,6-trifluorobenzene (Oakwood Products, Inc.) were dissolved in 150 mL dry ethyl ether. The solution was cooled to −78° C. in an acetone/dry-ice bath, then treated with 62.7 mL n-butyllithium (2 M solution in hexanes) over a two-hour period. Stirring was continued for 3 hours at −78° C. Via syringe, 34.8 g perfluorocyclohexanone were added, and the mixture was stirred at room temperature for 16 hours. The reaction was quenched with dilute HCl and extracted with ethyl ether, and the extracts were dried (using MgSO4) and rotary evaporated. Vacuum distillation (118-120° C., 80-110 Pa) gave 37.3 g 1-(3,5-dichloro-2,4,6-trifluorophenyl) perfluorocyclohexanol (62% yield) as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288266B1
Source datasetuspto-grants-2001_09
ORD IDord-6f5eba2e786348eb8a405b893cf87b86
Source noteuspto-grants-2001_09