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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156341Generated: November 1, 2026

Thionyl Chloride → HCID 13476546, compound

https://huagongshe.com/reaction/1156341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 20278969HCID 20278969—
SolventChloroformHCID 6212—
ProductHCID 13476546HCID 13476546—

Reaction Steps

A mixture of 8 parts of 3,4-dihydro-3-(2-hydroxyethyl)-4-methyl-2(1H)-quinazolinone, 8 parts of thionyl chloride and 90 parts of trichloromethane is stirred and refluxed for 1.50 hours. The reaction mixture is evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is stirred in 2,2'-oxybispropane. The product is filtered off and dried, yielding 6.6 parts of 3-(2-chloroethyl)-3,4-dihydro-4-methyl-2(1H)-quinazolinone; mp. 126.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04335127
Source datasetuspto-grants-1982_06
ORD IDord-213172111be84b469fc21e08b4233232
Source noteuspto-grants-1982_06