Imidazole → 5-O-[tert-butyl(diphenyl)silyl]-D-arabinofuranose

HRID 83995

반응식

HRID 83995 반응식
[O:1]=[CH:2][C@H:3]([C@@H:5]([C@@H:7]([CH2:9][OH:10])[OH:8])[OH:6])[OH:4].N1C=CN=C1.[C:16]([Si:20]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)Cl)([CH3:19])([CH3:18])[CH3:17]>CN(C)C=O>[Si:20]([O:1][CH2:2][C@H:3]1[O:4][CH:9]([OH:10])[C@@H:7]([OH:8])[C@@H:5]1[OH:6])([C:16]([CH3:19])([CH3:18])[CH3:17])([C:28]1[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1)[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1

참가 물질

5

실험 절차

D-Arabinose (200 g) and imidazole (199 g) were placed in a three-neck round bottom flask and connected to high vacuum for 30 minutes. The vacuum was released under nitrogen atmosphere and dimethylformamide (1.8 L) was added to the above mixture at room temperature followed by drop-wise addition of t-butyldiphenylchlorosilane (443 mL) for 10 minutes under a nitrogen atmosphere. The resulting mixture was stirred for 16 hours at the same temperature. Dimethylformamide was evaporated under reduced pressure. The residue was taken up in ethyl acetate and washed with water. The organic layer was dried over anhydrous sodium sulphate. The solvent was evaporated under reduced pressure to obtain a crude residue which was purified by column chromatography over silica gel using 80% ethyl acetate in hexane as eluant to afford the title compound (273 g).

후처리

  1. customDimethylformamide was evaporated under reduced pressure
  2. washwashed with water
  3. dry with materialThe organic layer was dried over anhydrous sodium sulphate
  4. customThe solvent was evaporated under reduced pressure
  5. customto obtain a crude residue which
  6. customwas purified by column chromatography over silica gel using 80% ethyl acetate in hexane as eluant

출처 및 근거

ORD 기록
ord-27b2e77f54ea48fc8e43c324e87fda9e
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08846910B2

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