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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Butanol | HCID 263 | — |
| 반응물 | Dopamine Hydrochloride | HCID 65340 | — |
| 반응물 | N-benzyloxycarbonyl-p-toluidinoacetaldehyde diethyl acetal | HCID 20460580 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1-(N-benzyloxycarbonyl-p-toluidinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 20460590 | 63.4% |
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
| 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-450ae31ddfe24a7bb4c2f7e67aba0817 |
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| 출처 메모 | uspto-grants-1980_09 |
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