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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489913Generated: October 29, 2026

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

https://huagongshe.com/reaction/1489913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(difluoromethyl)-2-carboxy-4-(p-fluorophenyl)butyrateHCID 15342052—
SolventWaterHCID 962—
Product(E)-2-(fluoromethylene)-4-(p-fluorophenyl)butan-1-olHCID 10943450—

Reaction Conditions

Temperature25 °C

Reaction Steps

Cool to 0° C.-10° C. a toluene solution of ethyl 2-(difluoromethyl)-2-carboxy-4-(p-fluorophenyl)butyrate as prepared in Example 4.1. Add water (396 kg) and a 50% by weight aqueous solution of sodium hydroxide. Stir for 30 minutes. Separate the aqueous layer and cool the aqueous layer to 0° C.-5° C. Add tetrahydrofuran (421 kg). Stir for hour at 0° C. and then warm to 25° C. and stir for 3 hours. Separate the aqueous layer. Evaporate the organic layer in vacuo at a temperature of 40° C.-50° C. The evaporation is continued until tetrahydrofuran no longer comes over and then toluene is added. Evaporate in vacuo until there is no longer water visible in the condensate. Concentrate in vacuo to give the title compound as a 80-90% by weight solution in toluene. An analytical sample prepared by evaporation of solvent gave 1H NMR (CDCl3, 300 MHz) δ 1.28 (t, J=7.2Hz 3H), 2.58 (m, 2H), 2.71 (m, 2H) 4.21 (q, J=7.2Hz, 2H), 6.93 (m, 2H), 7.15 (m, 2H), 7.51 (d, J=81.9Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05679854
Source datasetuspto-grants-1997_10
ORD IDord-6d676833cfd642af9e3e5d15ecf9fccc
Source noteuspto-grants-1997_10