Water → 2-(4-Bromo-2-methylphenyl)acetonitrile

HRID 859660노트

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HRID 859660 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8]Br)=[C:4]([CH3:10])[CH:3]=1.[C-:11]#[N:12].[Na+].O.C([O-])(O)=O.[Na+]>CN(C=O)C.CCOC(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:11]#[N:12])=[C:4]([CH3:10])[CH:3]=1

참가 물질

7

실험 절차

To a solution of 4-bromo-1-bromomethyl-2-methyl-benzene (3.96 g, 15 mmol) dissolved in DMF (16 mL) were added sodium cyanide (0.85 g, 17.25 mmol) and water (1.8 mL). The reaction was stirred for overnight at room temperature. To the reaction was added 100 mL water; 80 mL saturated NaHCO3, and 100 mL EtOAc. The layers were separated, and the aqueous layer was extracted with 3×100 mL EtOAc. The combined organics were washed with 100 mL water, and then dried over Na2SO4. After filtering off the solids, the mother liquor was concentrated to the desired product by rotary evaporation (2.92 g, 92.7% yield). 1H NMR (400 MHz, CDCl3): δ 2.32 (2 H, s), 3.62 (1 H, s), 7.20–7.27 (1 H, m), 7.32–7.41 (1 H, m).

후처리

  1. customThe layers were separated
  2. extractionthe aqueous layer was extracted with 3×100 mL EtOAc
  3. washThe combined organics were washed with 100 mL water
  4. dry with materialdried over Na2SO4
  5. filtrationAfter filtering off the solids
  6. concentrationthe mother liquor was concentrated to the desired product by rotary evaporation (2.92 g, 92.7% yield)

출처 및 근거

ORD 기록
ord-d3861953180c4806b5c55e638a06a7aa
출처 데이터셋
uspto-grants-2006_12
특허 번호
US07151105B2

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