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Dimethylformamide → HCID 17989247, 화합물

HRID 1444540
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HRID 1444540 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]#N)=[CH:4][C:3]=1[O:11][CH3:12].[CH3:13]I.[H-].[Na+].C[N:18]([CH3:21])C=O>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:13])([CH3:9])[C:21]#[N:18])=[CH:4][C:3]=1[O:11][CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 179892962-(4-Fluoro-3-methoxyphenyl)acetonitrile

생성물 1

HCID 17989247HCID 17989247, 화합물

실험 절차

16.67 g (100.93 mmol) of (4-fluoro-3-methoxyphenyl)-acetonitrile is introduced with 30.1 g (211.96 mmol) of methyliodide into 158 ml of dimethylformamide. At 0° C., 8.50 g (211.96 mmol) of a 55-60% sodium hydride suspension is added in portions. After stirring overnight at room temperature, the reaction mixture is poured into ice water and then extracted three times with methyl tert-butyl ether. The combined organic extracts are washed with water and with brine. After the solvent is dried and spun off, the residue is chromatographed on silica gel (mobile solvent ethyl acetate/hexane). 5.11 g (26.2%) of the desired compound and 6.18 g of the monomethyl compound, which is realkylated, are isolated.

후처리

  1. extractionextracted three times with methyl tert-butyl ether
  2. washThe combined organic extracts are washed with water and with brine
  3. customAfter the solvent is dried
  4. customthe residue is chromatographed on silica gel (mobile solvent ethyl acetate/hexane)
  5. customare isolated

출처 및 근거

ORD 기록
ord-5022b93d39234536b8b209e27fa8ed2b
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07662821B2

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