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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254428Generated: November 1, 2026

Benzoyl chloride → HCID 19744583, compound

https://huagongshe.com/reaction/2254428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium HydroxideHCID 14798—
Reactant3-(dimethoxymethyl)anilineHCID 232571—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 19744583HCID 1974458387.3%

Reaction Steps

1.06 g of 3-aminobenzaldehyde dimethyl acetal was dissolved in a mixture of 5 ml of toluene and 10 ml of water containing 0.8 g of sodium hydroxide, and 5 ml of a toluene solution of 1.3 g of benzoyl chloride was added. The mixture was stirred at room temperature for 2 hours. The organic layer was separated, and evaporated under reduced pressure. The residue was dissolved in a mixture of 10 ml of methanol and 10 ml of 10% hydrochloric acid, and heated at 90° C. for 30 minutes. Water (20 ml) was added to the reaction mixture to allow it to cool. There was obtained 1.16 g (yield 87.3%) of 3-benzoylaminobenzaldehyde as colorless needles having a melting point of 122° to 123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05234946
Source datasetuspto-grants-1993_08
ORD IDord-7fe8b96733cb4b6c9cec21a19597e21d
Source noteuspto-grants-1993_08