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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 973045생성일: 2026년 10월 24일

Acetic Acid → HCID 13121507, 화합물

https://huagongshe.com/ko/reaction/973045

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrochloric AcidHCID 313—
반응물2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamideHCID 290223—
반응물Sodium ethoxideHCID 2723922—
촉매SodiumHCID 5360545—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물HCID 13121507HCID 13121507—

반응 단계

A suspension of 392 g. (2.0 mole) of 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide and 321.2 g. (2.2 mole) of diethyl oxylate in 5 l. of absolute ethanol is added to a solution of sodium ethoxide, prepared from 50.6 g. (2.2 g. atoms) of sodium, in 2 l. of absolute ethanol under nitrogen. The mixture is stirred with heating at the reflux temperature for 6 hrs. and then refrigerated overnight. It is then diluted with stirring 15 l. with cool water. A finely divided precipitate forms which is removed by filtration. The filtrate is carefully acidified with 150 g. (2.5 mole) of acetic acid dissolved in 350 ml. of water. The resulting product which precipitates is collected on a filter, washed with water and air dried to yield 194.6 g. (0.7 mole) of the product of Procedure 2. The filtrate is acidified to pH 2 with concentrated hydrochloric acid and the resulting precipitate is collected on a filter, washed with water and air dried to give 264.8 g. (0.99 mole) of the desired product. A portion thereof weighing 25 g. is recrystallized from 1.4 l. of dioxane, yield 18.2 g., m.p. 223.5°-224.5° C. (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04054656
출처 데이터셋uspto-grants-1977_10
ORD IDord-9a4da07c488849e2a62b81430e6c542a
출처 메모uspto-grants-1977_10