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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650457Generated: November 3, 2026

Formic Acid → Ethyl 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetate

https://huagongshe.com/reaction/1650457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantEthyl 2-(2-tritylaminothiazol-4-yl)-2-allyloxyiminoacetateHCID 54525939—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetateHCID 5420961482.9%

Reaction Steps

A solution of ethyl 2-(2-tritylaminothiazol-4-yl)-2-allyloxyiminoacetate (syn isomer, 8.7 g.), 50% formic acid (42.5 ml.) and tetrahydrofuran (42.5 ml.) was stirred at 60° C. for 40 minutes. After concentrating the resultant solution in vacuo, the residue was dissolved in ethyl acetate, washed with an aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in turn, and dried over magnesium sulfate. After concentrating the resultant solution in vacuo, the residue was subjected to column chromatography on silica gel with benzene and ethyl acetate in turn, to give ethyl 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetate (syn isomer, 3.7 g.), mp. 102° to 104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923998
Source datasetuspto-grants-1990_05
ORD IDord-8d9c0bb59ae54d51ab15d531ad72be25
Source noteuspto-grants-1990_05