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Hydrochloric Acid → Ethyl 4-trimethylsilyl-3-cyanobutanoate

HRID 341336
ノート
印刷プレビュー

反応式

HRID 341336 の反応式
[C:1]([C:3]([CH2:15][Si:16]([CH3:19])([CH3:18])[CH3:17])([CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])C(OCC)=O)#[N:2].O.[Br-].[Li+].Cl>CN(C)C=O>[CH3:19][Si:16]([CH3:17])([CH3:18])[CH2:15][CH:3]([C:1]#[N:2])[CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11]
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 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 82050Lithium BromideHCID 71530806Diethyl 2-cyano-2-(trimethylsilylmethyl)succinate

生成物 1

HCID 71530807Ethyl 4-trimethylsilyl-3-cyanobutanoate収率 91%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
150 °C

実験手順

A solution of diethyl 2-cyano-2-(trimethylsilylmethyl)succinate (592 mg, 2.08 mmol) in dimethylformamide (DMF, 5 ml) was added with water (45 μl, 2.50 mmol) and lithium bromide (217 mg, 2.49 mmol), and the mixture was stirred at 150° C. for 15 hours. The reaction mixture was cooled on ice, and added with aqueous hydrochloric acid (1 N), and the mixture was extracted with ethyl acetate. The organic layer was washed with water, and then dried over anhydrous sodium sulfate, and the solvent was evaporated. The residue was purified by silica gel chromatography [hexane/ethyl acetate (14:1)] to obtain ethyl 4-trimethylsilyl-3-cyanobutanoate (404 mg, 91%) mentioned in the title as colorless oil.

後処理

  1. temperatureThe reaction mixture was cooled on ice
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe organic layer was washed with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. customthe solvent was evaporated
  6. customThe residue was purified by silica gel chromatography [hexane/ethyl acetate (14:1)]

出典と根拠

ORDレコード
ord-1f3d300b4af94f09892317d660713c12
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08895769B2

反応ノート

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