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Hydrochloric Acid → Ethyl 4-trimethylsilyl-3-cyanobutanoate

HRID 341336
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HRID 341336 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

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

생성물 1

HCID 71530807Ethyl 4-trimethylsilyl-3-cyanobutanoate수율 91%

시약·촉매·용매 1

HCID 6228Dimethylformamide
용매

반응 조건

온도
150 °C

실험 절차

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.

후처리

  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)]

출처 및 근거

ORD 기록
ord-1f3d300b4af94f09892317d660713c12
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895769B2

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