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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27148생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/27148

반응식

참여 물질

역할이름HCID투입량
반응물1-ButanolHCID 263—
반응물Dopamine HydrochlorideHCID 65340—
반응물N-benzyloxycarbonyl-p-chloroanilinoacetaldehyde diethyl acetalHCID 20460579—
용매WaterHCID 962—
생성물1-(N-benzyloxycarbonyl-p-chloroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 20460510111.3%

반응 단계

N-benzyloxycarbonyl-p-chloroanilinoacetaldehyde diethyl acetal (10 g) and 3,4-dihydroxyphenethylamine hydrochloride (4.2 g) were added to a mixture of n-butyl alcohol (100 ml) and water (14 ml) and then the mixture was refluxed for 4 hours. The above-mentioned acetal (1 g) was added to the mixture and the resultant mixture was refluxed for 4 hours. The reaction mixture was concentrated to dryness under reduced pressure and the residue was washed with ethyl acetate and collected by filtration. The crystals were recrystallized from a mixture of methanol and ether to give 1-(N-benzyloxycarbonyl-p-chloroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (7.0 g), mp 210° to 212° C. (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04220647
출처 데이터셋uspto-grants-1980_09
ORD IDord-29324dd202c84c9b9e0a37545ed7a11b
출처 메모uspto-grants-1980_09