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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethyl 5-methoxy-3-methyl-1-benzofuran-2-carboxylate → Ethyl 5-hydroxy-3-methyl-1-benzofuran-2-carboxylate

HRID 606582
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인쇄 미리보기

반응식

HRID 606582 반응식
[CH3:1][C:2]1[C:6]2[CH:7]=[C:8]([O:11]C)[CH:9]=[CH:10][C:5]=2[O:4][C:3]=1[C:13]([O:15][CH2:16][CH3:17])=[O:14]>ClCCl>[CH3:1][C:2]1[C:6]2[CH:7]=[C:8]([OH:11])[CH:9]=[CH:10][C:5]=2[O:4][C:3]=1[C:13]([O:15][CH2:16][CH3:17])=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 2307798Ethyl 5-methoxy-3-methyl-1-benzofuran-2-carboxylate

생성물 1

HCID 42883413Ethyl 5-hydroxy-3-methyl-1-benzofuran-2-carboxylate

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

Ethyl 3-methyl-5-methoxybenzofuran carboxylate (8.53 mmol) was dissolved in dichloromethane (10 ml) and a 1.0 M solution of boron tribromide methyl sulphide complex in dichloromethane (25.59 mmol) was added. The mixture was heated at reflux over night. The solvent was evaporated under vacuo and the residue purified by flash chromatography to obtain ethyl 3-methyl-5-hydroxybenzofuran carboxylate as a white solid.

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux over night
  3. customThe solvent was evaporated under vacuo
  4. customthe residue purified by flash chromatography

출처 및 근거

ORD 기록
ord-6ebdd579a1994699bfb77be6cea168e5
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07915300B2

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