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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethyl 7-(benzyloxy)-1h-indole-2-carboxylate → Ethyl 7-hydroxy-1H-indole-2-carboxylate

HRID 1762940
노트
인쇄 미리보기

반응식

HRID 1762940 반응식
[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[CH:10][C:9]=2[O:15]CC1C=CC=CC=1)=[O:5])[CH3:2]>[Pd].C(O)C>[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[CH:10][C:9]=2[OH:15])=[O:5])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 13242189Ethyl 7-(benzyloxy)-1h-indole-2-carboxylate

생성물 1

HCID 13093608Ethyl 7-hydroxy-1H-indole-2-carboxylate수율 86.2%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

One gram of 10% palladium catalyst on active carbon is added to a solution of 22.2 g of 7-benzyloxyindole-2-carboxylic acid ethyl ester in 500 ml of ethanol and the mixture is hydrogenated for 1 hour with shaking under normal pressure. The reaction solution is then filtered and the filtrate evaporated to dryness under vacuum. The residue is recrystallized from ethanol, yielding 13.3 g of 7-hydroxyindole-2-carboxylic acid ethyl ester, mp 197°-199° C.

후처리

  1. filtrationThe reaction solution is then filtered
  2. customthe filtrate evaporated to dryness under vacuum
  3. customThe residue is recrystallized from ethanol

출처 및 근거

ORD 기록
ord-92218c549768458d905c1f9975c48643
출처 데이터셋
uspto-grants-1989_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04835175

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