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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894771Generated: November 1, 2026

Methanol → 2-(2-Aminothiazol-4-yl)-2-(2,4-dichlorobenzyloxyimino)acetic acid

https://huagongshe.com/reaction/894771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1-MethylimidazoleHCID 1390—
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl 2-(2-aminothiazol-4-yl)-2-(2,4-dichlorobenzyloxyimino)acetateHCID 54440018—
SolventSodium HydroxideHCID 14798—
Product2-(2-Aminothiazol-4-yl)-2-(2,4-dichlorobenzyloxyimino)acetic acidHCID 5407645390.1%

Reaction Steps

A solution of 1-methylimidazole (0.5 g.) in 1 N sodium hydroxide aqueous solution (48 ml.) was added to a solution of ethyl 2-(2-aminothiazol-4-yl)-2-(2,4-dichlorobenzyloxyimino)acetate (syn isomer, 12.0 g.), methanol (120 ml.) and tetrahydrofuran (100 ml.) at 15° to 20° C., and stirred at 35° to 40° C. for 6 hours. After removing methanol and tetrahydrofuran in vacuo from the resultant mixture, the aqueous residue was washed with ethyl acetate. Ethyl acetate was completely removed from the aqueous solution and adjusted to pH 2.0 with hydrochloric acid. The precipitates were collected by filtration to give 2-(2-aminothiazol-4-yl)-2-(2,4-dichlorobenzyloxyimino) acetic acid (syn isomer, 10.0 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284631
Source datasetuspto-grants-1981_08
ORD IDord-eca19347c7f34db7945a71c40ec2d642
Source noteuspto-grants-1981_08