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Sodium Cyanide → (1-Pyridin-2-yl-cyclopentyl)-acetonitrile

HRID 2169464
ノート
印刷プレビュー

反応式

HRID 2169464 の反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1([CH2:12]OS(C)(=O)=O)[CH2:11][CH2:10][CH2:9][CH2:8]1.[C-:18]#[N:19].[Na+]>CS(C)=O>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1([CH2:12][C:18]#[N:19])[CH2:11][CH2:10][CH2:9][CH2:8]1
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

4

反応物 2

HCID 8929Sodium CyanideHCID 86726091Methanesulfonic acid 1-pyridin-2-yl-cyclopentylmethyl ester

生成物 1

HCID 86726092(1-Pyridin-2-yl-cyclopentyl)-acetonitrile収率 82.1%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

反応条件

温度
140 °C

実験手順

To a stirred solution of methanesulfonic acid 1-pyridin-2-yl-cyclopentylmethyl ester (433) (2 g, 7.843 mmol) in dimethyl sulfoxide (15 mL), KI (0.13 g, 0.784 mmol), NaCN (0.769 g, 15.686 mmol) were added and the reaction was subjected to heating at 140° C. for 5 h. The reaction mixture was quenched with ice cold water (50 mL) and extracted with ethyl acetate (2×70 mL). The combined extracts were washed with brine, dried and concentrated. The resulting crude product was purified by normal silica gel (100-200 mesh) column chromatography using 15% ethyl acetate in hexane as eluent to get (1-pyridin-2-yl-cyclopentyl)-acetonitrile (434) (1.2 g, 82%) as a colorless liquid.

後処理

  1. customThe reaction mixture was quenched with ice cold water (50 mL)
  2. extractionextracted with ethyl acetate (2×70 mL)
  3. washThe combined extracts were washed with brine
  4. customdried
  5. concentrationconcentrated
  6. customThe resulting crude product was purified by normal silica gel (100-200 mesh) column chromatography

出典と根拠

ORDレコード
ord-11e8526af7434962991d2fd8ed533215
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09045486B2

反応ノート

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