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

HRID 1624857
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HRID 1624857 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].C1C(=O)N([Br:22])C(=O)C1.O>CN(C=O)C>[Br:22][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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 67184N-bromobutanimideHCID 3199323-(3,4-Dimethoxyphenyl)propanenitrile

생성물 1

HCID 3204113-(2-Bromo-4,5-dimethoxyphenyl)propanenitrile

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
0 °C

실험 절차

A solution of 1 g (5.3 mmoles) of 3-(3,4-dimethoxyphenyl)propanenitrile in 42 mL of DMF is cooled to 0° C. To the resulting solution there is added, little by little, 0.93 g of NBS (5.2 mmoles, 1 eq.). After stirring for 30 minutes at 0° C., the reaction mixture is brought back to ambient temperature and stirred for two hours. It is then hydrolysed using 170 mL of water and extracted twice with 130 mL of ethyl acetate. The organic phases are collected and then washed, first with saturated aqueous Na2S2O5 solution and then with water. After evaporating off the solvent under reduced pressure, 1.29 g of a colourless oil which crystallises into a white solid are obtained.

후처리

  1. additionTo the resulting solution there is added
  2. customis brought back to ambient temperature
  3. stirringstirred for two hours
  4. extractionextracted twice with 130 mL of ethyl acetate
  5. customThe organic phases are collected
  6. washwashed, first with saturated aqueous Na2S2O5 solution
  7. customAfter evaporating off the solvent under reduced pressure, 1.29 g of a colourless oil which
  8. customcrystallises into a white solid
  9. customare obtained

출처 및 근거

ORD 기록
ord-a655c0a9287149348456602ed37746f2
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08779121B2

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