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Imidazole → 5-chloro-6-[(triisopropylsilyl)oxy]-1,3-benzoxazol-2(3H)-one

HRID 270130
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HRID 270130 반응식
[Cl:1][C:2]1[C:3]([OH:12])=[CH:4][C:5]2[O:9][C:8](=[O:10])[NH:7][C:6]=2[CH:11]=1.N1C=CN=C1.[CH:18]([Si:21](Cl)([CH:25]([CH3:27])[CH3:26])[CH:22]([CH3:24])[CH3:23])([CH3:20])[CH3:19]>CN(C)C=O>[Cl:1][C:2]1[C:3]([O:12][Si:21]([CH:25]([CH3:27])[CH3:26])([CH:22]([CH3:24])[CH3:23])[CH:18]([CH3:20])[CH3:19])=[CH:4][C:5]2[O:9][C:8](=[O:10])[NH:7][C:6]=2[CH:11]=1
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참가 물질

5

반응물 3

HCID 795ImidazoleHCID 27346-HydroxychlorzoxazoneHCID 139400Triisopropylsilyl chloride

생성물 1

HCID 689628865-chloro-6-[(triisopropylsilyl)oxy]-1,3-benzoxazol-2(3H)-one수율 85%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

5-chloro-6-hydroxy-1,3-benzoxazol-2(3H)-one (0.93 g, 5 mmol) and imidazole (1.00 g, 15 mmol) were dissolved in dimethylformamide (10 mL) with stirring under inert atmosphere. Triisopropylsilylchloride (1.15 g, 6 mmol) was added and the resulting solution was stirred for 3 days. The reaction mixture was partitioned between water and heptane. The organic layer was washed with water and dried over magnesium sulphate, filtrated and concentrated, to give 1.45 g (85%) of the subtitled compound as a grey solid.

후처리

  1. stirringthe resulting solution was stirred for 3 days
  2. customThe reaction mixture was partitioned between water and heptane
  3. washThe organic layer was washed with water
  4. dry with materialdried over magnesium sulphate
  5. filtrationfiltrated
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-c79150d587fc43059eb8de52887fbb0e
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07449475B2

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