Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489915Generated: October 31, 2026

Hydrochloric Acid → (E)-2-(fluoromethylene)-4-(p-fluorophenyl)butan-1-ol

https://huagongshe.com/reaction/1489915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactantethyl (E)-2-(fluoromethylene)-4-(p-fluorophenyl)butyrateHCID 15342053—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventWaterHCID 962—
Product(E)-2-(fluoromethylene)-4-(p-fluorophenyl)butan-1-olHCID 10943450—

Reaction Steps

Cool to 0° C. a solution of diisobutylaluminum hydride (7.64 kg, 25% by weight in toluene, 13.42 mol). Add a solution of ethyl (E)-2-(fluoromethylene)-4-(p-fluorophenyl)butyrate (1.74 kg, 74.1% by weight in toluene, 5.37 mol) at such a rate that the temperature of the reaction mixture does not rise above 20° C. After the addition is complete, warm to ambient temperature. After 2 hours, cool to 0° C. Slowly, add methanol (7.73 kg) at such a rate that the temperature of the reaction mixture does not rise above 15° C. Cool to 0° C. Slowly, add water (7.96 kg) at such a rate that the temperature of the reaction mixture does not rise above 20° C. Add a concentrated aqueous solution of hydrochloric acid (7.59 kg). Warm to ambient temperature. Separate the organic layer and dry azeotropically by distillation in vacuo until the volume of the organic layer is about one half of its original volume to give the title compound as a solution in toluene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05679854
Source datasetuspto-grants-1997_10
ORD IDord-ea219fa95c5748a5816c14b26e7a522e
Source noteuspto-grants-1997_10