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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3-Furancarboxylic acid, 5-methyl-2-phenyl-, ethyl ester → 5-Methyl-2-phenylfuran-3-carboxylic acid

HRID 2398665
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반응식

HRID 2398665 반응식
[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[C:4]([C:13]([O:15]CC)=[O:14])[CH:3]=1>[OH-].[Na+].C(O)C>[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[C:4]([C:13]([OH:15])=[O:14])[CH:3]=1
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참가 물질

4

반응물 1

HCID 100597273-Furancarboxylic acid, 5-methyl-2-phenyl-, ethyl ester

생성물 1

HCID 7610205-Methyl-2-phenylfuran-3-carboxylic acid

시약·촉매·용매 2

HCID 702Ethanol용매HCID 14798Sodium Hydroxide용매

실험 절차

Saponification of 0.5 g of the ester was accomplished by refluxing 12 hours in 10 ml of 25% aqueous sodium hydroxide and 5 ml of ethanol. Acidification precipitated the crude acid, which was recrystallized from water-ethanol to give 5-methyl-2-phenyl-3-furoic acid, mp 146°-147.5° C.

후처리

  1. customAcidification precipitated the crude acid, which
  2. customwas recrystallized from water-ethanol

출처 및 근거

ORD 기록
ord-51024104c9c6412fa0774d943abb5260
출처 데이터셋
uspto-grants-1977_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04025537

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