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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439203Generated: November 1, 2026

Aniline → alpha-Hydroxyacetophenone

https://huagongshe.com/reaction/1439203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantBenzanilideHCID 7168—
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 12823444HCID 12823444—
Productalpha-HydroxyacetophenoneHCID 68490—
ProductHCID 4070889HCID 4070889—

Reaction Steps

In a third method the 1,2-diphenylquinolones (IV, m = 0) are prepared by acylation of an appropriate aniline with an appropriate benzoyl chloride, chlorination of the resulting benzanilide, reaction of the benzimidoyl chloride so obtained with an appropriate 2-hydroxyacetophenone and rearrangement of the resulting 2-acetylphenyl N-phenylbenzimidate. The sequence of reactions is illustrated by the following equations: ##STR9##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04058532
Source datasetuspto-grants-1977_11
ORD IDord-b42d6539d0d04fe29d0ae593162f6ee0
Source noteuspto-grants-1977_11