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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663594Generated: October 29, 2026

Hydrochloric Acid → (4-Chlorophenyl)(4-cyanophenyl)methanol

https://huagongshe.com/reaction/1663594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantHCID 178467826HCID 178467826—
SolventCarbon dioxide methanolHCID 21973728—
Product(4-Chlorophenyl)(4-cyanophenyl)methanolHCID 6700108096%

Reaction Steps

To a solution of 4-cyanobenzaldehyde (3.93 g) in tetrahydrofaran was added dropwise 1.0M 4-chlorophenylmagnesium bromide-diethylether (30 mL) under nitrogen gas atmosphere and cooling in dry ice/methanol bath and the mixture was stirred at the same temperature for 10 minutes. To the reaction mixture was added 10% HCl solution and the aqueous layer was extracted with ethyl acetate (×2). The organic layer was washed with a saturated brine, dried over magnesium sulfate and concentrated in vacuo. To the resultant crude product was added diisopropyl ether and the resultant solid materials were collected by filtration to give (4-chlorophenyl)(4-cyanophenyl)methanol (6.98 g, yield: 96%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034949B2
Source datasetuspto-grants-2011_10
ORD IDord-79a58ad7274a4720b057ffb930410173
Source noteuspto-grants-2011_10