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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1585214생성일: 2026년 10월 27일

Ethanol → Ethyl 4,5,6,7-tetrahydro-1H-benzo[d]imidazole-6-carboxylate

https://huagongshe.com/reaction/1585214

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sulfate IonHCID 1117—
반응물Ethyl 1H-benzimidazole-6-carboxylateHCID 13505555—
촉매HCID 178418390HCID 178418390—
용매HCID 178418361HCID 178418361—
생성물Ethyl 4,5,6,7-tetrahydro-1H-benzo[d]imidazole-6-carboxylateHCID 21222281—

반응 단계

A mixture of 10.0 g of sulfate of benzimidazole-5-carboxylic ethyl ester, 5.0 g of 5% palladium-carbon catalyst, and 100 ml of ethanol was stirred in hydrogen for five hours under the conditions of 135° C. and 50 kg/cm2, cooled, then filtered to separate the catalyst, and distilled to expel the ethanol. The residue of the distillation was neutralized with an aqueous sodium bicarbonate solution and extracted with chloroform. The chloroform layer was dried over anhydrous magnesium sulfate and then distilled to expel chloroform and obtain 6.9 g of 4,5,6,7-tetrahydrobenzimidazole-5-carboxylic ethyl ester. This ester and 200 ml of 6N hydrochloric acid added thereto were refluxed together for seven hours. The hydrochloric acid solution was concentrated to dryness, crystallized by addition of acetone, separated by filtration, and then dried to obtain 6.9 g of hydrochloride of 4,5,6,7-tetrahydrobenzimidazole-5-carboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05936098
출처 데이터셋uspto-grants-1999_08
ORD IDord-44eadcf7d79240e28e635913ec9e072a
출처 메모uspto-grants-1999_08