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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 237124생성일: 2026년 10월 24일

Acetic Acid → HCID 13121507, 화합물

https://huagongshe.com/ko/reaction/237124

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 to 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 번호US04159377
출처 데이터셋uspto-grants-1979_06
ORD IDord-4f12f4109b654e34810204d18727d3c9
출처 메모uspto-grants-1979_06