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Phthalic Anhydride → 3-[(3-Methoxyphenyl)methylidene]-2-benzofuran-1(3H)-one

HRID 840499
노트
인쇄 미리보기

반응식

HRID 840499 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:9][C:10]([OH:12])=O)[CH:6]=[CH:7][CH:8]=1.C1(=O)O[C:16](=[O:17])[C:15]2=[CH:19][CH:20]=[CH:21][CH:22]=[C:14]12>C([O-])(=O)C.[Na+]>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:6]=[CH:7][CH:8]=1)[CH:9]=[C:10]1[C:19]2[C:15](=[CH:14][CH:22]=[CH:21][CH:20]=2)[C:16](=[O:17])[O:12]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6811Phthalic AnhydrideHCID 15719(3-Methoxyphenyl)acetic acid

생성물 1

HCID 544728733-[(3-Methoxyphenyl)methylidene]-2-benzofuran-1(3H)-one수율 69.7%

시약·촉매·용매 1

HCID 517045Sodium Acetate촉매

반응 조건

온도
240 °C

실험 절차

A mixture of 15 g (89 mmol) of m-methoxyphenyl acetic acid, 13.2 g (89 mmol) of phthalic anhydride and 246 mg (2.9 mmol) of sodium acetate was heated to 240° C. for 6 hours and water was continuously removed from the reaction. The solid formed in the reaction flask on cooling. This was recrystallized from absolute ethanol to obtain 15.6 g (62 mmol, 69%) of 1 as yellow powder.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. customwater was continuously removed from the reaction
  2. customThe solid formed in the reaction flask
  3. temperatureon cooling
  4. customThis was recrystallized from absolute ethanol

출처 및 근거

ORD 기록
ord-64bd66f01e48450f9d07b723ff12e19a
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06368814B1

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