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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263607Generated: October 25, 2026

Ammonia → 3-amino-5(N-methyl-allyloxycarbamoyl)-benzoic acid allyl ester

https://huagongshe.com/reaction/1263607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantStannous chloride dihydrateHCID 61436—
Reactant3-(N-methyl-allyloxycarbamoyl)-5-nitro-benzoic acid allyl esterHCID 22986100—
SolventEthyl AcetateHCID 8857—
Product3-amino-5(N-methyl-allyloxycarbamoyl)-benzoic acid allyl esterHCID 2298614199.6%

Reaction Steps

A mixture of (8(b)) (0.523 g), tin(II) chloride dihydrate (1.84 g) and ethyl acetate (50 ml) was heated under reflux for 6 hours. The mixture was allowed to cool to ambient temperature and ammonia solution (sp. g. 0.880) was added dropwise until the solution reached pH 8. The white precipitate which had formed was filtered off. washed with ethyl acetate (2×50 ml) and the combined washings and filtrate evaporated to dryness to give the desired starting material (8(c)) as a yellow oil (0.472 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541491B1
Source datasetuspto-grants-2003_04
ORD IDord-831059d1189841e79c57983a6cc92942
Source noteuspto-grants-2003_04