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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267956Generated: October 26, 2026

Thionyl Chloride → (2-Chlorophenyl)(4-chlorophenyl)methyl chloride

https://huagongshe.com/reaction/2267956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(2-Chlorophenyl)(4-chlorophenyl)methanolHCID 247332—
SolventChloroformHCID 6212—
Product(2-Chlorophenyl)(4-chlorophenyl)methyl chlorideHCID 247330102.3%

Reaction Steps

A stirred solution of 9.0 grams (0.036 mole) of (2-chlorophenyl)(4-chlorophenyl)methanol in 90 mL of chloroform was cooled to 0° C., and 5.3 mL (0.072 mole) of thionyl chloride was added. Upon completion of the addition the reaction mixture was allowed to warm to ambient temperature, where it stirred for about 18 hours. After this time the reaction mixture was filtered and concentrated under reduced pressure. The filtrate was taken up in hexane and subjected to column chromatography on silica gel with hexane as eluant. The product-containing fractions were combined and concentrated under reduced pressure, yielding 10.0 grams of (2-chlorophenyl)(4-chlorophenyl)methyl chloride. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSH0002007H1
Source datasetuspto-grants-2001_12
ORD IDord-a81c024108954c3da6b384adb0a4da93
Source noteuspto-grants-2001_12