Ethyl 2-(2-methyl-1,3-dioxolan-2-yl)butanoate → 2-(2-Methyl-[1,3]dioxolan-2-yl)-butan-1-ol

HRID 12485

反応式

HRID 12485 の反応式
C([O:3][C:4](=O)[CH:5]([C:8]1([CH3:13])[O:12][CH2:11][CH2:10][O:9]1)[CH2:6][CH3:7])C.[H-].[H-].[H-].[H-].[Li+].[Al+3]>CCOCC>[CH3:13][C:8]1([CH:5]([CH2:6][CH3:7])[CH2:4][OH:3])[O:9][CH2:10][CH2:11][O:12]1

参加物

4

実験手順

2-(2-Methyl-[1,3]dioxolan-2-yl)-butyric acid ethyl ester (85.5 g) was taken up in dry Et2O (50 mL). This mixture was added dropwise to a suspension of LiAlH4 (16.1 g) in dry Et2O (200 mL), cooled in an ice bath. The mixture was refluxed for 4 h., cooled in an ice bath, and quenched by adding H2O (16.1 mL), 2M aqueous NaOH (32.2 mL) and again H2O (16.1 mL). The suspension was filtered, the filter cake was washed with Et2O, and the combined filtrates were evaporated to dryness. The residue (49 g) was purified by vacuum distillation (112-125° C., 15 mbar), yielding 43.5 g of a clear, colorless liquid. 1H NMR (400 MHz, CDCl3) δ 0.98 (t, J=7.5 Hz, 3H), 1.10-1.24 (m, 1H), 1.31 (s, 3H), 1.50-1.75 (m, 2H), 3.12, (br s, 1H), 3.59-3.76 (m, 2H), 3.94-4.02 (m, 4H).

後処理

  1. temperaturecooled in an ice bath
  2. temperatureThe mixture was refluxed for 4 h.
  3. temperaturecooled in an ice bath
  4. customquenched
  5. additionby adding H2O (16.1 mL), 2M aqueous NaOH (32.2 mL) and again H2O (16.1 mL)
  6. filtrationThe suspension was filtered
  7. washthe filter cake was washed with Et2O
  8. customthe combined filtrates were evaporated to dryness
  9. distillationThe residue (49 g) was purified by vacuum distillation (112-125° C., 15 mbar)
  10. customyielding 43.5 g of a clear, colorless liquid

出典と根拠

ORDレコード
ord-fcb3b7df7fec4410b638d2761073fb52
出典データセット
uspto-grants-2010_06
特許番号
US07728018B2

関連ノート

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