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Lithium Hydroxide → 1-Methyl-2-oxocyclopentane-1-carbonitrile

HRID 1408936
ノート
印刷プレビュー

反応式

HRID 1408936 の反応式
[OH-].[Li+].I[CH3:4].[O:5]=[C:6]1[CH2:10][CH2:9][CH2:8][CH:7]1[C:11]#[N:12]>O.CO>[CH3:4][C:7]1([C:11]#[N:12])[CH2:8][CH2:9][CH2:10][C:6]1=[O:5]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 3939Lithium HydroxideHCID 6328Methyl iodideHCID 989302-Oxocyclopentane-1-carbonitrile

生成物 1

HCID 132142491-Methyl-2-oxocyclopentane-1-carbonitrile収率 78.3%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

反応条件

温度
50 °C

実験手順

A solution of lithium hydroxide (0.2226 g, 9.30 mmol) in water (5 mL) and iodomethane (0.591 mL, 9.46 mmol) were added to a stirred solution of 2-oxocyclopentanecarbonitrile (0.86 g, 7.88 mmol) in methanol (5 mL) at room temperature. The resulting mixture was heated to 50° C. for 1.5 h. The methanol solvent was removed in vacuo. The aqueous residue was extracted with ether (2×25 mL). The combined ether extracts were dried (Na2SO4), decanted and concentrated to give 1-methyl-2-oxocyclopentanecarbonitrile (0.76 g, 78% yield). 1H NMR (500 MHz, chloroform-d) δ ppm 2.63-2.74 (1 H, m), 2.43 (2 H, t, J=7.21 Hz), 1.59-1.93 (4 H, m), 1.34 (3 H, d, J=6.94 Hz).

後処理

  1. customThe methanol solvent was removed in vacuo
  2. extractionThe aqueous residue was extracted with ether (2×25 mL)
  3. dry with materialThe combined ether extracts were dried (Na2SO4)
  4. customdecanted
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-9b5c2db5b88b4cbebd1f28d8243e934d
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08921368B2

反応ノート

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