Butyric Acid → 2,2-Dimethoxyethyl butyrate

HRID 39251

反応式

HRID 39251 の反応式
[C:1]([OH:6])(=[O:5])[CH2:2][CH2:3][CH3:4].[CH3:7][O:8][CH:9]([O:12][CH3:13])[CH2:10]Br.C([O-])([O-])=O.[K+].[K+].O>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.CC#N>[C:1]([O:6][CH2:10][CH:9]([O:12][CH3:13])[O:8][CH3:7])(=[O:5])[CH2:2][CH2:3][CH3:4]

参加物

7

反応条件

温度
134 °C

実験手順

A mixture of butyric acid (1.0 g, 11.35 mmol), bromoacetaldehyde dimethyl acetal (2.25 mL, 19.13 mmol), tetrabutylammonium bromide (1.83 g, 5.67 mmol) and K2CO3 (1.56 g, 11.35 mmol) in 10 mL of anhydrous CH3CN was stirred at 134° C. for 16 h in a sealed tube. It was cooled to room temperature, water was added and the mixture was extracted with Et2O (3×120 mL). The combined organic phases were washed with saturated NaCl (2×60 mL), dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography on silica gel using 20-30% ethyl acetate/hexanes to give the product 43a (1.56 g, 78%). 1H NMR (400 MHz, CDCl3) δ 0.90 (t, J=7.43 Hz, 3H), 1.60 (sextet, J=7.43, 7.04 Hz, 2H), 2.24 (t, J=7.04 Hz, 2H), 3.36 (s, 6H), 4.08 (d, J=5.3 Hz, 2H), 4.54 (t, J=5.3 Hz, 1H).

後処理

  1. temperatureIt was cooled to room temperature
  2. extractionthe mixture was extracted with Et2O (3×120 mL)
  3. washThe combined organic phases were washed with saturated NaCl (2×60 mL)
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by flash chromatography on silica gel using 20-30% ethyl acetate/hexanes

出典と根拠

ORDレコード
ord-5d5ededb485a4de2877448b0b3b2ec91
出典データセット
uspto-grants-2013_09
特許番号
US08524691B2

関連ノート

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