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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 284115, 화합물 → HCID 20452411, 화합물

HRID 1462959
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HRID 1462959 반응식
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]=[CH:9][C:10]([C:12]1[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=1)=[O:11].[BH4-].[Na+]>C(O)C>[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH2:9][CH:10]([C:12]1[CH:13]=[CH:14][C:15]([O:18][CH3:19])=[CH:16][CH:17]=1)[OH:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 284115HCID 284115, 화합물HCID 4311764Sodium borohydride

생성물 1

HCID 20452411HCID 20452411, 화합물수율 66.7%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2-Hydroxy-4'-methoxychalcone (12.7 g) was stirred with ethanol (200 ml) and sodium borohydride (3.8 g) added in portions. The solution was stirred at room temperature, the solvent evaporated, and the residue washed with water and recrystallised from aqueous ethanol to give 3-(o-hydroxyphenyl)-1-(p-methoxyphenyl)propan-1-ol (8.60 g), m.p. 114°-116°. The total product was boiled under reflux with acetic acid (100 ml) for 2 hr., the solution evaporated, and the residue chromatographed on alumina, eluting with toluene, to yield 4'-methoxyflavan (8.0 g), m.p. 82°-83°.

후처리

  1. additionadded in portions
  2. customthe solvent evaporated
  3. washthe residue washed with water
  4. customrecrystallised from aqueous ethanol

출처 및 근거

ORD 기록
ord-7cfe63c84dff4b2f82102abcfee3e8a6
출처 데이터셋
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04461907

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