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Hydrochloric Acid → HCID 15922632, 화합물

HRID 1247548
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HRID 1247548 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:11])=[C:6]([CH2:8][C:9]#N)[CH:7]=1.[CH3:12]I.[H-].[Na+].Cl.C[N:18]([CH3:21])C=O>C(OCC)(=O)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:11])=[C:6]([C:8]([CH3:12])([CH3:9])[C:21]#[N:18])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 6228DimethylformamideHCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 27746255-Fluoro-2-methylphenylacetonitrile

생성물 1

HCID 15922632HCID 15922632, 화합물

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

5.25 g of (5-fluoro-2-methylphenyl)acetonitrile and 5.25 ml of methyl iodide are dissolved in 70 ml of dimethylformamide and mixed with 2.7 g of sodium hydride (80%) for 2.5 hours while being cooled with ice. After 3 hours at 0° C. and 16 hours at room temperature, it is mixed with ice water and ethyl acetate, acidified with 1 M hydrochloric acid, and the ethyl acetate phase is washed with water, dried (Na2SO4) and concentrated by evaporation. 6.1 g of 2-(5-fluoro-2-methylphenyl)-2-methylpropionitrile is obtained as an oil.

후처리

  1. temperaturewhile being cooled with ice
  2. washthe ethyl acetate phase is washed with water
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated by evaporation

출처 및 근거

ORD 기록
ord-77d75c0f405c45178ce5dc7dcdc8a3a3
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07129270B2

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