Benzene → 3-[N-(alpha-chloroacetyl)-2-methyl-4-chloroanilino]propionaldehyde

HRID 1576941노트

반응식

HRID 1576941 반응식
[CH3:1][C:2]1[CH:12]=[C:11]([Cl:13])[CH:10]=[CH:9][C:3]=1[NH:4][CH2:5][CH2:6][CH:7]=[O:8].C1C=CC=CC=1.C(=O)([O-])[O-].[Na+].[Na+].[Cl:26][CH2:27][C:28](Cl)=[O:29]>O>[Cl:26][CH2:27][C:28]([N:4]([CH2:5][CH2:6][CH:7]=[O:8])[C:3]1[CH:9]=[CH:10][C:11]([Cl:13])=[CH:12][C:2]=1[CH3:1])=[O:29]

참가 물질

6

실험 절차

The diethyl acetal of 3-(2-methyl-4-chloroanilino)propionaldehyde (0.2 mole), benzene (150 ml) and sodium carbonate (0.2 mole) dissolved in water (50 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and addition funnel. The mixture is cooled in an ice bath and chloroacetyl chloride (0.2 mole) is added dropwise with stirring. After addition is completed stirring is continued and the reaction mixture is allowed to warm up to room temperature. After this time the mixture is filtered and the filtrate washed with dilute aqueous hydrochloric acid. The washed filtrate is dried over anhydrous magnesium sulphate and is stripped of solvent under reduced pressure to yield the desired product the diethyl acetal of 3-[N-(α-chloroacetyl)-2-methyl-4-chloroanilino]propionaldehyde.

후처리

  1. additionare charged into a glass reaction vessel
  2. customequipped with a mechanical stirrer
  3. additionthermometer and addition funnel
  4. temperatureThe mixture is cooled in an ice bath
  5. additionAfter addition
  6. stirringis completed stirring
  7. filtrationAfter this time the mixture is filtered
  8. washthe filtrate washed with dilute aqueous hydrochloric acid
  9. dry with materialThe washed filtrate is dried over anhydrous magnesium sulphate

출처 및 근거

ORD 기록
ord-cce2c93df68940aaa0229d13e320629c
출처 데이터셋
uspto-grants-1976_09
특허 번호
US03983174

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