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

HRID 1624857
ノート
印刷プレビュー

反応式

HRID 1624857 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
0 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-a655c0a9287149348456602ed37746f2
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08779121B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート