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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27146생성일: 2026년 10월 24일

1-Butanol → 1-(N-benzyloxycarbonyl-p-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

https://huagongshe.com/ko/reaction/27146

반응식

참여 물질

역할이름HCID투입량
반응물1-ButanolHCID 263—
반응물Dopamine HydrochlorideHCID 65340—
반응물N-benzyloxycarbonyl-p-fluoroanilinoacetaldehyde diethyl acetalHCID 20460532—
용매WaterHCID 962—
생성물1-(N-benzyloxycarbonyl-p-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 2046054244.6%

반응 단계

N-benzyloxycarbonyl-p-fluoroanilinoacetaldehyde diethyl acetal (6 g) and 3,4-dihydroxyphenethylamine hydrochloride (2.5 g) were added to a mixture of n-butyl alcohol (60 ml) and water (8.5 ml). The mixture was then refluxed for 11 hours in a stream of nitrogen. In the course of the reaction, amounts of the above-mentioned acetal (0.6 g and 1.2 g) were added to the mixture after 4.5 hours and 6 hours, respectively, from the beginning of the reaction. The reaction mixture was concentrated to dryness and the residue was washed with ether and dissolved in water. The solution was washed with ether and concentrated to dryness to give amorphous 1-(N-benzyloxycarbonyl-p-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (2.7 g), mp 122° C. (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04220647
출처 데이터셋uspto-grants-1980_09
ORD IDord-5ff7cb659ce54ae3ac8a4d37277a9d40
출처 메모uspto-grants-1980_09