Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28263Generated: October 25, 2026

Hydrochloric Acid → (2-Chlorophenyl)(4-chlorophenyl)methanol

https://huagongshe.com/reaction/28263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-ChlorobenzaldehydeHCID 6996—
Reactantp-BromochlorobenzeneHCID 7806—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product(2-Chlorophenyl)(4-chlorophenyl)methanolHCID 247332—

Reaction Steps

To 12.7 g. (0.52 moles) of magnesium turnings in 200 ml. of anhydrous ether is added 10.0 g. (0.052 moles) of p-bromochlorobenzene, and the mixture is warmed to reflux. When the Grignard reaction begins, the heat is removed and 80.0 g. (0.47 moles) of additional p-bromochlorobenzene in 80 ml. of ether is added dropwise as the refluxing continues. When the addition is completed, the reaction is heated at reflux for 2 hours, cooled, and 73.4 g. (0.52 moles) of o-chlorobenzaldehyde are slowly added. The reaction is refluxed for 2 hours, cooled and poured into iced water. The resulting mixture is made acidic with hydrochloric acid, and the organic phase is separated. The aqueous layer is extracted with ether, and the extract is added to the organic phase. This solution is washed with water, dried over anhydrous magnesium sulfate and concentrated to give an oily solid. The material is crystallized from petroleum ether to give 109.4 g. (83%) of the product, mp 68°-70°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04225723
Source datasetuspto-grants-1980_09
ORD IDord-d1fb74da1fe1496a9557c93116c7aab5
Source noteuspto-grants-1980_09