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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284708Generated: October 28, 2026

Tetrahydrofuran → 2-(2-Aminothiazol-4-yl)-2-allyloxyiminoacetic acid

https://huagongshe.com/reaction/1284708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetateHCID 54209614—
SolventMethanolHCID 887—
Product2-(2-Aminothiazol-4-yl)-2-allyloxyiminoacetic acidHCID 5448425359.6%

Reaction Steps

A solution of ethyl 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetate (syn isomer, 3.6 g.), 2N aqueous solution of sodium hydroxide (14.1 ml.), tetrahydrofuran (14.1 ml.) and methanol (15 ml.) was stirred at 40° C. for 1.5 hours. The resultant solution was concentrated in vacuo, and the residue was dissolved in water. After the solution was adjusted to pH 2.8 with 10% hydrochloric acid under ice cooling, the precipitates were collected by filtration, washed with water and acetone in turn and dried to give 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetic acid (syn isomer, 1.91 g.), mp. 187° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04563522
Source datasetuspto-grants-1986_01
ORD IDord-27a072dc1794477f9d33fb539a8ed7cc
Source noteuspto-grants-1986_01