ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Acetaminophen → N-[4-[(5-Bromopentyl)oxy]phenyl]acetamide

HRID 222419
ノート
印刷プレビュー

反応式

HRID 222419 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][CH2:15][CH2:16][CH2:17]Br.C(=O)([O-])[O-].[K+].[K+]>CC(CC)=O.C(Cl)(Cl)Cl>[Br:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][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 81001,5-DibromopentaneHCID 11430Potassium Carbonate

生成物 1

HCID 12355860N-[4-[(5-Bromopentyl)oxy]phenyl]acetamide収率 72.15%

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, 0.01 mol) and 1,5-dibromopentane (9) (10.0 ml) in ethyl methyl ketone (25.0 ml) containing potassium carbonate (5.0 g) was stirred for 8 hr 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% sodium hydroxide solution (3×100 ml), water (3×50 ml), dried, filtered and crystallized from methanol to get the desired product N-[4-(5-bromo-pentoxy)-phenyl]-acetamide (11) (2.15 g, 72.15%), mp 110-111° 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% sodium hydroxide 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-c5d8c8f81a9045f3802240306d1ccb34
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

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート