Dimethyl Sulfoxide → Ethyl 2-(1-cyanocyclohexyl)acetate

HRID 846404ノート

反応式

HRID 846404 の反応式
[CH3:1][O:2][C:3](=[O:17])[CH:4]([C:9]1([C:15]#[N:16])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1)C(OC)=O.[Cl-].[Li+].O.[CH3:21]S(C)=O>>[CH2:1]([O:2][C:3](=[O:17])[CH2:4][C:9]1([C:15]#[N:16])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1)[CH3:21]

参加物

5

実験手順

26.9 g (100 mmol) of (1-cyanocyclohexyl)malonic acid dimethyl ester, 4.3 g (100 mmol) or lithium chloride and 3.6 g (200 mmol) of water were heated in 300 ml of dimethyl sulfoxide for 22 hours to 150° C. Then it was cooled, mixed with 700 ml of water and extracted with 1000 ml of pentane. 14.4 g of (1-cyanocyclohexyl)acetic acid ethyl ester was obtained by distillation of the organic phase, corresponding to a yield of 74 percent (relative to the (1-cyanocyclohexyl)malonic acid dimethyl ester used). Data for the product was:

後処理

  1. temperatureThen it was cooled
  2. extractionextracted with 1000 ml of pentane

出典と根拠

ORDレコード
ord-d375a53009ed485c8f87ab38ddf99739
出典データセット
uspto-grants-1992_08
特許番号
US05136091

反応ノート

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