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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156343Generated: November 2, 2026

Thionyl Chloride → HCID 13476542, compound

https://huagongshe.com/reaction/1156343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 13476541HCID 13476541—
ProductHCID 13476542HCID 1347654286%

Reaction Steps

A mixture of 3.6 parts of 1-(2-hydroxyethyl)-2,4(1H,3H)-quinazolinedione and 40 parts of thionyl chloride is stirred and refluxed overnight. The reaction mixture is allowed to cool to room temperature. The precipitated product is filtered off, washed with 2,2'-oxybispropane and dried, yielding 3.4 parts (86%) of 1-(2-chloroethyl)-2,4-(1H,3H)-quinazolinedione; mp. 215.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04335127
Source datasetuspto-grants-1982_06
ORD IDord-c5da8d98a7164fa885d9ed1288adb209
Source noteuspto-grants-1982_06