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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1440836생성일: 2026년 10월 27일

Hydrochloric Acid → 1H-Indole-3-ethanamine, 7-chloro-

https://huagongshe.com/reaction/1440836

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-Chlorophenylhydrazine hydrochlorideHCID 443287—
반응물2-(4,4-Diethoxybutyl)isoindoline-1,3-dioneHCID 12805186—
용매EthanolHCID 702—
생성물1H-Indole-3-ethanamine, 7-chloro-HCID 145709—

반응 단계

A 10.0 g sample of 2-chlorophenylhydrazine hydrochloride and 17.9 g of 4-phthalimidobutyraldehyde diethyl acetal were stirred in 200 mL ethanol with 1 mL 5N HCl. The mixture was concentrated to a residue which was slurried in a small amount of methylene chloride. A yellow solid was collected and vacuum dried at 40° C. The solid was stirred in 500 mL ethanol. Hydrazine hydrate (14 g) was added and the mixture was heated at reflux for 14 hours. A 60 mL sample of 5N HCl was added and the mixture was heated at reflux for 1 hour. The mixture was allowed to cool and was concentrated to a residue. The residue was partitioned between 1N NaOH and chloroform. The organic layer was separated and the aqueous layer was extracted with chloroform. The combined extracts were dried (Na2SO4) and concentrated to an oil. The oil was chromatographed on silica gel using a gradient of 0-10% methanol in chloroform containing 0.2% ammonium hydroxide. Fractions containing product were concentrated to an oil which was taken up in a small amount of methanol and added to ethereal HCl. A solid was collected, washed with diethyl ether, and vacuum dried at 50° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05500431
출처 데이터셋uspto-grants-1996_03
ORD IDord-2ffdad1e8a4149f399eaa8d73265f33d
출처 메모uspto-grants-1996_03