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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605657Generated: October 30, 2026

Isopropanol → (E)-4-(2-chloro-4-biphenylyl)-3-pentene-2-ol

https://huagongshe.com/reaction/1605657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantAluminum isopropoxideHCID 11143—
Reactant(E)-4-(2-chloro-biphenylyl)-3-pentene-2-oneHCID 68133289—
Product(E)-4-(2-chloro-4-biphenylyl)-3-pentene-2-olHCID 21547087—

Reaction Steps

80.0 Gm (0.296 mol) of (E)-4-(2-chloro-biphenylyl)-3-pentene-2-one were gently refluxed with 68.0 gm (0.333 mol) of aluminum isopropylate and 300 ml (3.92 mols) of isopropanol in a dry distillation apparatus with a 60-cm-Vigreux-column, such that only about 5 drops were distilled off per minute. After about 5 hours no acetone was found to be present in the distillate (using hydrochloric acid 2,4-dinitrophenyl-hydrazine solution) and in the reaction mixture no unreacted starting material could be found (by thin-layer-chromatography). The isopropanol was distilled off in a weak vacuum. The residue was hydrolyzed by addition of 300 gm of crushed ice. The ethereal (upper) phase, was decanted, and the aluminum hydrozide slurry was carefully washed with ether several times. The combined extracts were washed with water, with aqueous 5% sodium hydroxide and again with water, and dried over sodium sulfate. The solvent was evaporated in vacuo and the residue was recrystallized once from petroleum ether/ethyl acetate (ratio by volume = 4:1). Yield: 64.0 gm (79% of theory) of colorless crystals, m.p. 86°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03950427
Source datasetuspto-grants-1976_04
ORD IDord-df8a3c75c02c4349beb8bed63ebf6f85
Source noteuspto-grants-1976_04