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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Butanol | HCID 263 | — |
| 반응물 | Dopamine Hydrochloride | HCID 65340 | — |
| 반응물 | N-benzyloxycarbonyl-p-fluoroanilinoacetaldehyde diethyl acetal | HCID 20460532 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1-(N-benzyloxycarbonyl-p-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 20460542 | 44.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04220647 |
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| 출처 데이터셋 | uspto-grants-1980_09 |
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| ORD ID | ord-5ff7cb659ce54ae3ac8a4d37277a9d40 |
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| 출처 메모 | uspto-grants-1980_09 |
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