氯乙腈 → Cyanomethyl-(alpha-naphthylmethyl)-malonic acid diethyl ester

HRID 4589

反应方程式

HRID 4589 反应方程式
[C:1]([CH2:3]C(CC1C2C(=CC=CC=2)C=CC=1)C(O)=O)#[N:2].[CH2:19]([O:21][C:22](=[O:40])[CH:23]([CH2:29][C:30]1[C:39]2[C:34](=[CH:35][CH:36]=[CH:37][CH:38]=2)[CH:33]=[CH:32][CH:31]=1)[C:24]([O:26][CH2:27][CH3:28])=[O:25])[CH3:20].ClCC#N.[H-].[Na+]>CN(C=O)C>[CH2:27]([O:26][C:24](=[O:25])[C:23]([CH2:3][C:1]#[N:2])([CH2:29][C:30]1[C:39]2[C:34](=[CH:35][CH:36]=[CH:37][CH:38]=2)[CH:33]=[CH:32][CH:31]=1)[C:22]([O:21][CH2:19][CH3:20])=[O:40])[CH3:28]

参与物

6

实验过程

2(R,S)-Cyanomethyl-3-α-naphthylpropionic acid: 3.0 g of α-naphthylmethylmalonic acid diethyl ester and, after 30 minutes, 0.6 ml of chloroacetonitrile are added to a stirred suspension of 0.44 g of sodium hydride dispersion in 50 ml of DMF. The reaction mixture is stirred for 1 hour at 50° and then concentrated by evaporation in a high vacuum. The residue is dissolved in ethyl acetate, washed with 0.1N hydrochloric acid and water, dried over sodium sulphate, concentrated by evaporation and purified by chromatography on silica gel with toluene, yielding cyanomethyl-(α-naphthylmethyl)-malonic acid diethyl ester.

后处理

  1. concentrationconcentrated by evaporation in a high vacuum
  2. dissolutionThe residue is dissolved in ethyl acetate
  3. washwashed with 0.1N hydrochloric acid and water
  4. dry with materialdried over sodium sulphate
  5. concentrationconcentrated by evaporation
  6. custompurified by chromatography on silica gel with toluene

来源与证据

ORD记录
ord-e9adca82e09c421dacd1f2f89a865ee9
来源数据集
uspto-grants-1988_02
专利号
US04727060

关联笔记

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