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Water → 3-(2-Bromo-4,5-dimethoxyphenyl)propanenitrile

HRID 1624863
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HRID 1624863 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][CH2:12][C:13]#[N:14])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].C([O-])(=O)C.[Na+].[Br:20]Br.O>C(O)(=O)C>[Br:20][C:6]1[CH:7]=[C:8]([O:9][CH3:10])[C:3]([O:2][CH3:1])=[CH:4][C:5]=1[CH2:11][CH2:12][C:13]#[N:14]
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참가 물질

6

반응물 4

HCID 962WaterHCID 24408BromineHCID 3199323-(3,4-Dimethoxyphenyl)propanenitrileHCID 517045Sodium Acetate

생성물 1

HCID 3204113-(2-Bromo-4,5-dimethoxyphenyl)propanenitrile수율 65.1%

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

실험 절차

To a mixture of 21 g of 3-(3,4-dimethoxyphenyl)propanenitrile, 10.3 g of sodium acetate and 400 mL of acetic acid there are added 20 g of dibromine in 50 mL of acetic acid. The resulting reaction mixture is stirred overnight and then poured into water and extracted with benzene. The organic phase is washed with aqueous sodium thiosulphate solution and then with water, dried over sodium sulphate and concentrated under reduced pressure. The crude reaction product is purified on a silica column (eluant: benzene), and the product obtained is recrystallised from ethanol to yield 19.3 g of the expected product.

후처리

  1. customThe resulting reaction mixture
  2. extractionextracted with benzene
  3. washThe organic phase is washed with aqueous sodium thiosulphate solution
  4. dry with materialwith water, dried over sodium sulphate
  5. concentrationconcentrated under reduced pressure
  6. customThe crude reaction product
  7. customis purified on a silica column (eluant: benzene)
  8. customthe product obtained
  9. customis recrystallised from ethanol

출처 및 근거

ORD 기록
ord-382adc58b35b49a89d2035fecd30b336
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08779122B2

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