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Acetaminophen → N-[4-(3-bromopropoxy)phenyl]acetamide

HRID 1451642
ノート
印刷プレビュー

反応式

HRID 1451642 の反応式
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9](=[O:11])[CH3:10])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[Br:18][CH2:19][CH2:20][CH2:21]Br>CN(C=O)C>[Br:18][CH2:19][CH2:20][CH2:21][O:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][C:9](=[O:11])[CH3:10])=[CH:6][CH:7]=1
参加物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 1983AcetaminophenHCID 80011,3-DibromopropaneHCID 11430Potassium Carbonate

生成物 1

HCID 10849771N-[4-(3-bromopropoxy)phenyl]acetamide

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A mixture of N-(4-hydroxyphenyl)acetamide (10 g) and potassium carbonate (11 g) in DMF (200 ml) was stirred for 20 min at room temperature. 1,3-Dibromopropane (35 ml) was then added and stirring was continued for 4 h. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was treated with water and extracted with dichloromethane. The organic phase was washed first with dilute sodium hydroxide, then with water, dried and concentrated to give a solid which was triturated with hexane to give the title compound (14 g), MP: 120°.

後処理

  1. stirringstirring
  2. waitwas continued for 4 h
  3. filtrationThe mixture was filtered
  4. concentrationthe filtrate was concentrated in vacuo
  5. additionThe residue was treated with water
  6. extractionextracted with dichloromethane
  7. washThe organic phase was washed first with dilute sodium hydroxide
  8. dry with materialwith water, dried
  9. concentrationconcentrated
  10. customto give a solid which
  11. customwas triturated with hexane

出典と根拠

ORDレコード
ord-764df50af8924601b61364ae28220610
出典データセット
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05604237

反応ノート

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