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(2-Acetamidophenyl) cyclohexyl methanone → (2-Aminophenyl)(cyclohexyl)methanone

HRID 235240
ノート
印刷プレビュー

反応式

HRID 235240 の反応式
C([NH:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]([CH:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1)=[O:12])(=O)C>CO>[NH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]([CH:13]1[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18]1)=[O:12]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 11586813(2-Acetamidophenyl) cyclohexyl methanone

生成物 1

HCID 15634733(2-Aminophenyl)(cyclohexyl)methanone収率 91.1%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
80 °C

実験手順

A solution of (2-acetamidophenyl) cyclohexyl methanone (0.53 g, 2.16 mmol) in methanol (5 ml) and concentrated hydrochloric add (15 ml) was heated at 80° C. for 1 h. After this time the solution was cooled to ambient temperature and the solvents removed in vacuo. The residue was dissolved in water (10 ml) and basified with 4N sodium hydroxide solution (20 ml). The mixture was then extracted into ethyl acetate (4×20 ml) and the organic layers combined and dried (MgSO4). The solvent was evaporated and the residue chromatographed on silica gel, using petrol:ethyl acetate (2:1), to afford the amine (0.40 g, 91%) as a white solid. mp 73°-75° C. 1H NMR (360 MHz, CDCL3)-- 1.23-2.09 (10H, m), 3.27 (1H, m), 6.29 (2H, brs), 6.64 (2H, m), 7.25 (1H, dt, J=6 and 1 Hz), 7.76 (1H, dd, J -7 and 1 Hz).

後処理

  1. additionadd (15 ml)
  2. temperatureAfter this time the solution was cooled to ambient temperature
  3. customthe solvents removed in vacuo
  4. dissolutionThe residue was dissolved in water (10 ml)
  5. extractionThe mixture was then extracted into ethyl acetate (4×20 ml)
  6. dry with materialdried (MgSO4)
  7. customThe solvent was evaporated
  8. customthe residue chromatographed on silica gel

出典と根拠

ORDレコード
ord-b1e787aae57f427598a3ad39411cde6d
出典データセット
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05597915

反応ノート

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