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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47003Generated: October 25, 2026

Methanone, (2-chlorophenyl)phenyl- → 2-Chlorobenzhydrol, (+-)-

https://huagongshe.com/reaction/47003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanone, (2-chlorophenyl)phenyl-HCID 78838—
ReactantSodium borohydrideHCID 4311764—
SolventIsopropanolHCID 3776—
Product2-Chlorobenzhydrol, (+-)-HCID 23581976%

Reaction Steps

A mixture containing 15.0 g (0.0692 mole) of 2-chlorobenzophenone, 4.1 g (0.1094 mole) of sodium borohydride, and 200 ml of anhydrous isopropanol is heated to reflux and maintained at reflux until the reaction is complete (2.0 hours), as indicated by vpc techniques. The solvent is removed in vacuo, whereupon the residue is diluted with ether, washed with a dilute hydrochloric acid solution and with water until neutral, dried (magnesium sulfate), and concentrated in vacuo. Recrystallization of the resulting residue from petroleum ether affords 11.5 g (0.0526 mole) of 2-chlorobenzhydrol, m.p. 61°-63°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04175945
Source datasetuspto-grants-1979_11
ORD IDord-c2744ee57a024e7487d75f296a69f439
Source noteuspto-grants-1979_11