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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855983Generated: November 1, 2026

Benzoyl chloride → HCID 23347367, compound

https://huagongshe.com/reaction/1855983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantAmmonium thiocyanateHCID 15666—
ReactantHCID 713863HCID 713863—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
ProductHCID 23347367HCID 23347367—

Reaction Steps

The starting material is obtained as follows: A solution of 6 g ammonium thiocyanate in 200 ml acetone is treated with 7 ml benzoyl chloride and stirred for 10 minutes. To this solution 6 g of 4-chloro-5-amino-2,1,3-benzothiadiazole in 200 ml of methanol is added. The mixture is boiled for 2 hours and cooled yielding N-benzoyl-N'-(4-chloro-2,1,3-benzothiadiazol-5-yl)thiourea (M.Pt. 220°-222° from methanol). The precipitate was filtered off and quickly heated to reflux with 100 ml of a 2 N aqueous solution of sodium hydroxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04217356
Source datasetuspto-grants-1980_08
ORD IDord-9c1fffa8f3534d55aef5026b091c16ea
Source noteuspto-grants-1980_08