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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27145생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/27145

반응식

참여 물질

역할이름HCID투입량
반응물1-ButanolHCID 263—
반응물Dopamine HydrochlorideHCID 65340—
반응물N-benzyloxycarbonyl-p-toluidinoacetaldehyde diethyl acetalHCID 20460580—
용매WaterHCID 962—
생성물1-(N-benzyloxycarbonyl-p-toluidinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 2046059063.4%

반응 단계

N-benzyloxycarbonyl-p-toluidinoacetaldehyde 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) and then the mixture was refluxed for 9.5 hours in a stream of nitrogen. In the course of the reaction, the above-mentioned acetal (0.6 g) was twice added to the mixture, after 5 hours and after 7.5 hours from the beginning of the reaction. The reaction mixture was concentrated and the residue was washed with ether and dissolved in hot water (300 ml). After the insoluble material was filtered off, the filtrate was washed with ethyl acetate and treated with activated charcoal. The aqueous layer was concentrated to dryness to give amorphous 1-(N-benzyloxycarbonyl-p-toluidinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (3.8 g), mp 125° C. (dec).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04220647
출처 데이터셋uspto-grants-1980_09
ORD IDord-450ae31ddfe24a7bb4c2f7e67aba0817
출처 메모uspto-grants-1980_09