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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414504Generated: October 27, 2026

Ethanol → 1,1-Difluoro-2,2-dimethyl-3-(3-phenylamino-4-fluorobenzyloxy)propane

https://huagongshe.com/reaction/414504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium HydroxideHCID 14797—
Reactant1,1-Difluoro-2,2-dimethyl-3-[3-(N-phenyl-N-acetylamino)-4-fluorobenzyloxy]propaneHCID 21281089—
SolventWaterHCID 962—
Product1,1-Difluoro-2,2-dimethyl-3-(3-phenylamino-4-fluorobenzyloxy)propaneHCID 2128108052%

Reaction Steps

1,1-Difluoro-2,2-dimethyl-3-[3-(N-phenyl-N-acetylamino)-4fluorobenzyloxy]propane (0.5 g) was suspended in a 1 molar solution of potassium hydroxide in water containing 20% by volume ethanol and the mixture was heated at the reflux temperature for 8 hours. After standing overnight at the ambient temperature, the mixture was shaken several times with ethyl acetate and the combined organic extracts washed with water and brine, and dried over anhydrous magnesium sulphate. Evaporation of the solvent under reduced pressure gave a brown oil which was purified by column chromatography on a silica gel supoort, eluting with petroleum ether (boiling range 40°-60° C.) containing 10% by volume ethyl acetate, to give the title compound (0.23 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792563
Source datasetuspto-grants-1988_12
ORD IDord-a97baa1ff93c429eb52f47454fbbfa89
Source noteuspto-grants-1988_12