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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462594Generated: October 30, 2026

Water → Benzhydryl 2-t-butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetate

https://huagongshe.com/reaction/462594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantTert-Butyl nitriteHCID 10906—
ReactantBenzhydryl 2-t-butoxycarbonylmethoxyimino-2-(2-aminothiazol-4-yl)acetateHCID 53827226—
SolventTetrahydrofuranHCID 8028—
ProductBenzhydryl 2-t-butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetateHCID 5422379145.5%

Reaction Steps

A solution of t-butyl nitrite (1.7 g) in tetrahydrofuran (10 ml) was dropwise added to a solution of benzhydryl 2-t-butoxycarbonylmethoxyimino-2-(2-aminothiazol-4-yl)acetate (syn isomer) (5 g) in tetrahydrofuran (50 ml) at 50° to 53° C. under stirring and the mixture was stirred at the same temperature at 25 minutes. The reaction mixture was poured into a mixture of ethyl acetate and water and the organic layer was separated. The organic layer was washed with brine and dried over magnesium sulfate. The solution was evaporated and the residue was subjected to column chlomatography on silica gel. The elution was carried out with a mixture of benzene and ethyl acetate (19:1) and the eluates containing the object compound were evaporated to give benzhydryl 2-t-butoxycarbonylmethoxyimino-2-(4-thiazolyl)acetate (syn isomer) (2.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04515788
Source datasetuspto-grants-1985_05
ORD IDord-e221332a3a5444e3aac1a75f1113c757
Source noteuspto-grants-1985_05