Isopropanol → 1-Quinolin-6-ylcyclopropanecarbaldehyde

HRID 500148

反応式

HRID 500148 の反応式
[H-].C([Al+]CC(C)C)C(C)C.[N:11]1[C:20]2[C:15](=[CH:16][C:17]([C:21]3([C:24]#N)[CH2:23][CH2:22]3)=[CH:18][CH:19]=2)[CH:14]=[CH:13][CH:12]=1.C([OH:29])(C)C>C1(C)C=CC=CC=1.C(OCC)(=O)C>[N:11]1[C:20]2[C:15](=[CH:16][C:17]([C:21]3([CH:24]=[O:29])[CH2:23][CH2:22]3)=[CH:18][CH:19]=2)[CH:14]=[CH:13][CH:12]=1

参加物

6

反応条件

温度
-2.5 °C

実験手順

Diisobutylaluminum hydride (1M in THF, 96 mL, 96 mmol) was added to a solution of 1-quinolin-6-ylcyclopropanecarbonitrile (12.4 g, 63.9 mmol) in toluene (120 mL) at −78° C. under an atmosphere of nitrogen. The reaction mixture was allowed to warm to −5 to 0° C., and stirred at that temperature for 3 h. The reaction mixture was cooled to −60° C. Isopropyl alcohol (10 mL) was carefully added dropwise. After stirring for 30 min, the reaction mixture was warmed to −5 to 0° C. The reaction mixture was diluted with ethyl acetate, quenched with water and extracted with ethyl acetate. The combined organic extracts were washed with water, brine, dried over sodium sulfate, filtered through a pad of silica gel eluting with 40% ethyl acetate in hexanes. The filtrate was concentrated to yield the desired product. (12 g, 95.1%).

後処理

  1. temperatureThe reaction mixture was cooled to −60° C
  2. stirringAfter stirring for 30 min
  3. temperaturethe reaction mixture was warmed to −5 to 0° C
  4. customquenched with water
  5. extractionextracted with ethyl acetate
  6. washThe combined organic extracts were washed with water, brine
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered through a pad of silica gel eluting with 40% ethyl acetate in hexanes
  9. concentrationThe filtrate was concentrated

出典と根拠

ORDレコード
ord-c00962cf83ca495b81fd172efc6e1077
出典データセット
uspto-grants-2010_08
特許番号
US07767675B2

関連ノート

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