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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370023Generated: October 25, 2026

Methanol → 4-Amino-3-chloro-5-methoxyiminomethylbenzoic acid

https://huagongshe.com/reaction/370023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant4-Amino-3-chloro-5-methoxyiminomethylbenzoateHCID 73432822—
SolventWaterHCID 962—
Product4-Amino-3-chloro-5-methoxyiminomethylbenzoic acidHCID 5409913494%

Reaction Steps

In a 5-liter three-necked round-bottomed flask was placed 210 g (0.86 moles) of the previously prepared 4-amino-3-chloro-5-methoxyiminomethylbenzoate, 1.7 l of methanol and 462 g (1.73 moles) of 15% aqueous sodium hydroxide. The resulting mixture was refluxed for 3 hours, after which the reaction mixture was stirred overnight at room temperature. The reaction mixture was concentrated using a rotary evaporator. The crude reaction mixture was dissolved in 2 l of water. The resulting aqueous solution was washed once with 500 mL of ethyl acetate, cooled in an ice bath and acidified to pH=2 with concentrated hydrochloric acid. The expected 4-amino-3-chloro-5-methoxyiminomethylbenizoic acid precipitated as a light yellow solid which was separated by suction filtration. The filter cake was washed with a 1:2 mixture of ethyl ether and hexane yielding after drying 185.2 g (94% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140362
Source datasetuspto-grants-2000_10
ORD IDord-5a8fb1205e6f4ed38e76203e7a0d99f6
Source noteuspto-grants-2000_10