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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28282생성일: 2026년 10월 24일

Acetic Anhydride → Ethyl 2-(formylamino)-alpha-oxo-4-thiazoleacetate

https://huagongshe.com/ko/reaction/28282

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Potassium PermanganateHCID 516875—
반응물Ethyl 2-formamidothiazol-4-acetateHCID 688091—
반응물HCID 178470762HCID 178470762—
용매Acetic AcidHCID 176—
생성물Ethyl 2-(formylamino)-alpha-oxo-4-thiazoleacetateHCID 2733245—

반응 단계

A mixture of manganous acetate tetrahydrate (120 g.), acetic acid (1000 ml) and acetic anhydride (100 ml.) was stirred for 20 minutes in an oil bath heated at 130° to 135° C., and to the mixture was added potassium permanganate (20 g.) over 5 minutes at 105° to 110° C. with stirring and then the mixture was further stirred for 30 minutes at 130° to 135° C. The mixture was cooled to room temperature, and to the mixture was added ethyl 2-(2-formylaminothiazol-4-yl)acetate, which can be represented as ethyl 2-(2-formylimino-2,3-dihydrothiazol-4-yl)acetate, (53.5 g.), and then the mixture was stirred for 15 hours at 38° to 40° C. under introduction of air at the rate of 6000 ml. per minute. After the reaction, the precipitates were collected by filtration. The precipitates were washed with acetic acid and water in turn and then dried to give ethyl 2-(2-formylaminothiazol-4-yl)glyoxylate, which can be represented as ethyl 2-(2-formylimino-2,3-dihydrothiazol-4-yl)glyoxylate, (41.5 g.), mp 232° to 233° C. (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04225707
출처 데이터셋uspto-grants-1980_09
ORD IDord-7ccb5fd1af4b433096c4032ff4abacd9
출처 메모uspto-grants-1980_09