Acetonitrile → 4,4-Dimethyl-3-oxohexanenitrile

HRID 657839ノート

反応式

HRID 657839 の反応式
[H-].[Na+].[C:3](#[N:5])[CH3:4].C([O:8][C:9](=O)[C:10]([CH3:14])([CH3:13])[CH2:11][CH3:12])C>O1CCCC1.Cl>[CH3:13][C:10]([CH3:14])([CH2:11][CH3:12])[C:9](=[O:8])[CH2:4][C:3]#[N:5]

参加物

6

反応条件

温度
60 °C

実験手順

A suspension of sodium hydride (60% dispersion in mineral oil, 3.18 g, 79.4 mmol) in tetrahydrofuran (60 mL) was heated at 60° C. for 1 hour. The reaction mixture was then cooled to room temperature, acetonitrile (4.2 mL, 79.4 mmol) and 2,2-dimethyl-butyric acid ethyl ester [(7.95 g, 61 mmol), J. Am. Chem. Soc., 1942, 64, 2964] in tetrahydrofuran (100 mL) were added and the mixture was stirred for 4 hours at 25° C. The mixture was then diluted with 1M hydrochloric acid (100 mL) and the aqueous layer was separated and extracted with ethyl acetate. The organic solution was then dried over magnesium sulfate, concentrated in vacuo and the residue was triturated with heptane to afford the title compound as a pale brown solid in 27% yield, 2.3 g.

後処理

  1. temperatureThe reaction mixture was then cooled to room temperature
  2. customthe aqueous layer was separated
  3. extractionextracted with ethyl acetate
  4. dry with materialThe organic solution was then dried over magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customthe residue was triturated with heptane

出典と根拠

ORDレコード
ord-affeb2d86b2f40c6abc19030d4b6863c
出典データセット
uspto-grants-2011_12
特許番号
US08076356B2

反応ノート

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