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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895382Generated: October 30, 2026

Benzoyl chloride → Aniline

https://huagongshe.com/reaction/895382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 15908598HCID 15908598—
ReactantHCID 178523892HCID 178523892—
ProductAnilineHCID 6115—
ProductBenzhydrylamineHCID 7036—

Reaction Steps

N-[1-(2,4-Dichlorophenyl)-2-(imidazol-1-yl)-ethyl]-N′-phenyl)carbonyl thiourea. Compound A was prepared by following the procedure of Example 190, Step A, except benzoyl chloride was used instead of 4-chlorobenzoyl chloride. B. N-[1-(2,4-Dichlorophenyl)-2-(imidazol-1-yl)-ethyl]—N′-phenyl-N″-phenylcarbonylguanidine. Step B of Example 190 was followed using Compound A, above, and aniline (instead of diphenylmethylamine) to obtain Example 191. MS (ES): m/z 478 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916813B2
Source datasetuspto-grants-2005_07
ORD IDord-49ab3c0fb15146ed8515e83e9d9d940f
Source noteuspto-grants-2005_07