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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727779Generated: October 29, 2026

Hydrochloric Acid → 3,5-Dichloro-4-(4-chlorobenzoyl)benzyl alcohol

https://huagongshe.com/reaction/727779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3,5-Dichlorobenzylic alcoholHCID 43236—
Product3,5-Dichloro-4-(4-chlorobenzoyl)benzyl alcoholHCID 2817766—

Reaction Steps

Concentrated aqueous HCl (25 ml) is added to the above reaction mixture, which is allowed to warm to room temperature and aged for 12 hours. The reaction is monitored by silica gel TLC eluted with 10% EtOAc in hexane (Rf 5: 0.03). Upon completion the reaction mixture is partitioned between EtOAc (100 ml) and cold H2O (300 ml) and the layers are separated. The organic layer is washed with H2O (150 ml), 1N aqueous NaOH (2×150 ml, thoroughly to remove 4-chlorobenzoic acid), H2O (150 ml), and 0.1N aqueous HCl. The organic layer is dried (Na2SO4), filtered, and concentrated to give crude crystalline 3,5-dichloro-4-(4-chlorobenzoyl)-benzyl alcohol, 5 (9.97 g), 60 weight percent pure (70% assay yield from alcohol 2) by HPLC assay on DuPont Zorbax ODS-C8 eluted isocratically at ambient temperature at 2 ml/min with 55% H2O, 45% CH3CN, and 0.1% H3PO4 and monitored by UV detection at 230 mn (retention times, alcohol 2: 5.1 min; benzophenone 5: 14.4 min; 4-chlorobenzoic acid: 2.9 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045543
Source datasetuspto-grants-1991_09
ORD IDord-0d415fb50ee54057b900146774ede931
Source noteuspto-grants-1991_09