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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 893855생성일: 2026년 10월 25일

Methanol → 2-Tert-butoxycarbonyl-1,2,3,4-tetrahydro-benzo[b]thieno[2,3-c]pyridine-3-carboxylic acid

https://huagongshe.com/reaction/893855

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sodium HydroxideHCID 14798—
반응물2-Tert-butoxycarbonyl-1,2,3,4-tetrahydrobenzo[b]thieno[2,3-c]pyridine-carboxylic acid ethyl esterHCID 19960856—
용매ChloroformHCID 6212—
생성물2-Tert-butoxycarbonyl-1,2,3,4-tetrahydro-benzo[b]thieno[2,3-c]pyridine-3-carboxylic acidHCID 6995960675%

반응 단계

In a mixed solvent of 30 ml of methanol and 20 ml of chloroform was dissolved 6 g of 2-tert-butoxycarbonyl-1,2,3,4-tetrahydrobenzo[b]thieno[2,3-c]pyridine-carboxylic acid ethyl ester and 4 ml of an aqueous solution of 5N sodium hydroxide was further added thereto, and then the solution was refluxed for 5 hours. The solvents were distilled off under reduced pressure and 300 ml of 5% citric acid and 300 ml of chloroform were added to the residue. The chloroform layer was washed with a saturated aqueous sodium chloride solution and then dried by sodium sulfate. After distilling off chloroform under reduced pressure, the residue formed was recrystallized from a mixture of chloroform and hexane to provide 4.15 g (yield of 75%) of 2-tert-butoxycarbonyl-1,2,3,4-tetrahydrobenzo[b]thieno[2,3-c]pyridine-3-carboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05126448
출처 데이터셋uspto-grants-1992_06
ORD IDord-36cccc27ee4145db9b1c284e496830da
출처 메모uspto-grants-1992_06