n-Methyl-p-aminophenol → 4-[N-Methyl-N-(5-chloro-2-benzoxazolyl)amino]phenol

HRID 1446874ノート

反応式

HRID 1446874 の反応式
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][C:6]([OH:9])=[CH:5][CH:4]=1.C(=O)([O-])[O-].[K+].[K+].Cl[C:17]1[O:18][C:19]2[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][C:20]=2[N:21]=1.C(=O)([O-])[O-].[Na+].[Na+]>C(C(C)=O)C.O>[CH3:1][N:2]([C:3]1[CH:8]=[CH:7][C:6]([OH:9])=[CH:5][CH:4]=1)[C:17]1[O:18][C:19]2[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][C:20]=2[N:21]=1

参加物

7

反応物 4

HCID 5931n-Methyl-p-aminophenolHCID 10340Sodium CarbonateHCID 11430Potassium CarbonateHCID 103975782,5-Dichlorobenzooxazole

生成物 1

HCID 133148194-[N-Methyl-N-(5-chloro-2-benzoxazolyl)amino]phenol

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6569Methyl Ethyl Ketone溶媒2 回

実験手順

A solution of the sulfate salt of 4-(N-methylamino)phenol (0.008 mol, 2.76 g) in methyl ethyl ketone (25 ml) containing pure potassium carbonate (0.008 mol, 1.1 g) was warmed to reflux and a solution of 2,5-dichlorobenzoxazole (0.016 mol, 3.0 g) in methyl ethyl ketone (25 ml) was added dropwise over 2 hours. The resulting mixture was heated at reflux for a further hour, stood overnight, then stirred at room temperature for a further 8 hours. The solvent was then evaporated leaving a white solid. This was treated with a mixture of water (25 ml) and saturated aqueous sodium carbonate solution (25 ml). The solid was collected, washed with water, dried by suction and recrystallised three times from boiling toluene. Yield 1.4 g, mp 216°-217° C.; ir and pmr spectra and analysis consistent with assigned structure.

後処理

  1. temperaturewas warmed
  2. temperatureto reflux
  3. temperatureThe resulting mixture was heated
  4. temperatureat reflux for a further hour
  5. customThe solvent was then evaporated
  6. customleaving a white solid
  7. customThe solid was collected
  8. washwashed with water
  9. customdried by suction
  10. customrecrystallised three times

出典と根拠

ORDレコード
ord-361b7305a21046b298020cef63fa536d
出典データセット
uspto-grants-1982_02
特許番号
US04314065

反応ノート

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