Imidazole → (2R)-1-(benzyloxy)-3-[(triisopropylsilyl)oxy]-2-propanol

HRID 1496907ノート

反応式

HRID 1496907 の反応式
Cl[Si:2]([CH:9]([CH3:11])[CH3:10])([CH:6]([CH3:8])[CH3:7])[CH:3]([CH3:5])[CH3:4].[CH2:12]([O:19][CH2:20][C@@H:21]([OH:24])[CH2:22][OH:23])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.N1C=CN=C1>CN(C=O)C>[CH2:12]([O:19][CH2:20][C@@H:21]([OH:24])[CH2:22][O:23][Si:2]([CH:9]([CH3:11])[CH3:10])([CH:6]([CH3:8])[CH3:7])[CH:3]([CH3:5])[CH3:4])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

参加物

5

実験手順

Chloro(triisopropyl)silane (12.2 mL, 0.057 mol) was added dropwise at 20° C. to a stirred solution of diol 78 (9.52 g, 0.052 mol) and imidazole (5.33 g, 0.078 mol) in DMF (150 mL) and stirring was continued for 16 h. Most of the DMF was removed under reduced pressure and the residue was partitioned between EtOAc and water. The organic extract was washed well with water, then brine, and was evaporated to give an oil, which was chromatographed on silica. Elution with petroleum ether gave fore fractions, and then further elution with EtOAc/petroleum ether (1:19) gave (2R)-1-(benzyloxy)-3-[(triisopropylsilyl)oxy]-2-propanol (79) (13.80 g, 78%) as a colourless oil: [α]19 −0.78° (c, 8.93, CHCl3); 1H NMR (CDCl3) δ 7.41-7.27 (m, 5H), 4.55 (s, 2H), 3.90-3.84 (m, 1H), 3.79-3.72 (m, 2H), 3.59-3.51 (m, 2H), 2.52 (d, J=5.1 Hz, 1H), 1.13-1.03 (m, 21H). APCI MS m/z 339 [M+H]+.

後処理

  1. customMost of the DMF was removed under reduced pressure
  2. customthe residue was partitioned between EtOAc and water
  3. extractionThe organic extract
  4. washwas washed well with water
  5. custombrine, and was evaporated
  6. customto give an oil, which
  7. customwas chromatographed on silica
  8. washElution with petroleum ether
  9. customgave fore fractions
  10. washfurther elution with EtOAc/petroleum ether (1:19)

出典と根拠

ORDレコード
ord-1028d5faab6d4f63a4d0e149d101b6ba
出典データセット
uspto-grants-2015_12
特許番号
US09198913B2

反応ノート

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