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Acetic Anhydride → 5-(Trifluoromethyl)isobenzofuran-1,3-dione

HRID 328285
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반응식

HRID 328285 반응식
[F:1][C:2]([F:16])([F:15])[C:3]1[CH:4]=[C:5]([C:12]([OH:14])=[O:13])[C:6](=[CH:10][CH:11]=1)[C:7](O)=[O:8].C(OC(=O)C)(=O)C>>[F:1][C:2]([F:16])([F:15])[C:3]1[CH:4]=[C:5]2[C:12](=[O:14])[O:13][C:7](=[O:8])[C:6]2=[CH:10][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7918Acetic AnhydrideHCID 5990394-(Trifluoromethyl)phthalic acid

생성물 1

HCID 127177895-(Trifluoromethyl)isobenzofuran-1,3-dione수율 74.7%

실험 절차

4-Trifluoromethyl-phthalic acid (106.6 g.) and acetic anhydride (215 cc.) are heated to the reflux temperature for 30 minutes. After concentration under reduced pressure (30 mm Hg), the residue is stirred with cyclohexane (420 cc.). After filtration and drying, 4-trifluoromethyl-phthalic anhydride (73.5 g.) melting at 54° C is obtained.

후처리

  1. concentrationAfter concentration under reduced pressure (30 mm Hg)
  2. filtrationAfter filtration
  3. customdrying

출처 및 근거

ORD 기록
ord-6eae555cb5c84c91b3e011b3515d54ee
출처 데이터셋
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04016274

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