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

HRID 222420
ノート
印刷プレビュー

反応式

HRID 222420 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.[Br:12][CH2:13][CH2:14][CH:15](Br)C.C(=O)([O-])[O-].[K+].[K+]>CC(CC)=O.C(Cl)(Cl)Cl>[Br:12][CH2:13][CH2:14][CH2:15][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

6

反応物 3

HCID 1983AcetaminophenHCID 78891,3-DibromobutaneHCID 11430Potassium Carbonate

生成物 1

HCID 10849771N-[4-(3-bromopropoxy)phenyl]acetamide収率 75.8%

試薬・触媒・溶媒 2

HCID 6212Chloroform溶媒HCID 6569Methyl Ethyl Ketone溶媒

実験手順

A solution of N-(4-hydroxyphenyl)acetamide (paracetamol) (1) (1.50 g) and 1,3-dibromobutane (14) (10.0 ml) in ethyl methyl ketone (25.0 ml) containing potassium carbonate (5.0 g) was stirred overnight at room temperature. The reaction mixture was filtered, residue washed with ethyl methyl ketone and solvent evaporated under reduced pressure to get the residue. The residue was dissolved in chloroform (200.0 ml), washed with 5% NaOH solution (3×100 ml), water (3×50 ml), dried, filtered and crystallized from methanol to get the desired product N-[4-(3-Bromo-propoxy)-phenyl]-acetamide (16) (2.01 g, 75.8%), mp 115-118° C.

後処理

  1. filtrationThe reaction mixture was filtered
  2. washresidue washed with ethyl methyl ketone and solvent
  3. customevaporated under reduced pressure
  4. customto get the residue
  5. washwashed with 5% NaOH solution (3×100 ml), water (3×50 ml)
  6. customdried
  7. filtrationfiltered
  8. customcrystallized from methanol

出典と根拠

ORDレコード
ord-6a4785e6ef5844c69e7b5a35e512d58b
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08207222B2

反応ノート

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