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Potassium Hydroxide → p-(2,4-Dimethoxybenzyloxy)aniline

HRID 1448442
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HRID 1448442 반응식
[CH3:1][O:2][C:3]1[CH:20]=[C:19]([O:21][CH3:22])[CH:18]=[CH:17][C:4]=1[CH2:5][O:6][C:7]1[CH:16]=[CH:15][C:10]([NH:11]C(=O)C)=[CH:9][CH:8]=1.[OH-].[K+]>C(O)C>[CH3:1][O:2][C:3]1[CH:20]=[C:19]([O:21][CH3:22])[CH:18]=[CH:17][C:4]=1[CH2:5][O:6][C:7]1[CH:16]=[CH:15][C:10]([NH2:11])=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 20379816p-(2,4-Dimethoxybenzyloxy)acetanilide

생성물 1

HCID 20379808p-(2,4-Dimethoxybenzyloxy)aniline

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

p-(2,4-Dimethoxybenzyloxy)acetanilide (3 g, 0.01 M) in ethanol (30 ml) is treated with potassium hydroxide (3 g), then the mixture is heated under reflux for 12 hours. The solvent is removed by evaporation, the residue treated with water and extracted with ether. The ether solution is treated with charcoal, dried and concentrated to afford p-(2,4-dimethoxybenzyloxy)aniline.

후처리

  1. temperaturethe mixture is heated
  2. temperatureunder reflux for 12 hours
  3. customThe solvent is removed by evaporation
  4. additionthe residue treated with water
  5. extractionextracted with ether
  6. additionThe ether solution is treated with charcoal
  7. customdried
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-b8a49b87ed4243e9aa697cc303af4aa9
출처 데이터셋
uspto-grants-1979_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04180509

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