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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648839Generated: October 29, 2026

Trifluoroacetic acid → 2-t-Butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetic acid

https://huagongshe.com/reaction/648839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantEthyl AcetateHCID 8857—
ReactantBenzhydryl 2-t-butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetateHCID 54223791—
SolventDichloromethaneHCID 6344—
Product2-t-Butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetic acidHCID 5447273776.9%

Reaction Steps

To a solution of benzhydryl 2-t-butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetate (syn isomer) (2.2 g) and anisole (2.2 ml) in methylene chloride (22 ml) was added trifluoroacetic acid (4 ml) at ambient temperature and the mixture was stirred at the same temperature for 25 minutes. To the reaction mixture was added ethyl acetate and the solution was washed with water. To the separated organic layer was added water and the mixture was adjusted to pH 7.5 with 20% aqueous solution of sodium carbonate. The separated aqueous layer was acidified to pH 2.0 with 10% hydrochloric acid. The acidified solution was saturated with sodium chloride and extracted with ethyl acetate. The ethyl acetate layer was washed with brine, and dried over magnesium sulfate. The solution was evaporated and the residue was pulverized with diisopropyl ether and n-hexane to give 2-t-butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetic acid (syn isomer) (1.07 g), mp. 136°-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04736039
Source datasetuspto-grants-1988_04
ORD IDord-2fe3d611762245a288cbe5a395b2813c
Source noteuspto-grants-1988_04