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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Benzyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline → 1-Benzyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline

HRID 893325
노트
인쇄 미리보기

반응식

HRID 893325 반응식
[CH2:1]([CH:8]1[C:17]2[C:12](=[CH:13][C:14]([O:20]C)=[C:15]([O:18]C)[CH:16]=2)[CH2:11][CH2:10][NH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>Br>[CH2:1]([CH:8]1[C:17]2[C:12](=[CH:13][C:14]([OH:20])=[C:15]([OH:18])[CH:16]=2)[CH2:11][CH2:10][NH:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 300241-Benzyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

생성물 1

HCID 1775111-Benzyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline수율 83.2%

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

실험 절차

Treat 1-benzyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline (10 g) with 48% HBr (100 mL) and heat the mixture at reflux under nitrogen for 2 h. Cool the mixture to room temperature and allow crystals to form overnight. Collect the crystals and wash with cold ethanol to give 7.5 g of the title compound as its HBr salt, mp=233°-236° C.

후처리

  1. temperatureheat the mixture
  2. temperatureat reflux under nitrogen for 2 h
  3. customto form overnight
  4. customCollect the crystals
  5. washwash with cold ethanol

출처 및 근거

ORD 기록
ord-c9e1a9cce5a54e46a15f151c95fbf8b9
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05124337

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