Water → 4-Benzyloxybenzophenone

HRID 70735

反応式

HRID 70735 の反応式
[H-].[Na+].[OH:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:11])=[CH:6][CH:5]=1.[CH2:18](Br)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.O>CN(C=O)C>[CH2:18]([O:3][C:4]1[CH:5]=[CH:6][C:7]([C:10]([C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[O:11])=[CH:8][CH:9]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

参加物

6

反応物 4

HCID 962WaterHCID 7498Benzyl BromideHCID 143474-HydroxybenzophenoneHCID 24758Sodium hydride

生成物 1

HCID 4581934-Benzyloxybenzophenone

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

NaH (60% in mineral oil, 1.2 g, 30 mmol) was added to an ice-cooled solution of (4-hydroxy-phenyl)-phenyl-methanone (5 g, 25.2 mmol) in DMF (25 mL). Stirred for 20 minutes at room temperature. Benzyl bromide (6.1 ml, 50 mmol) was added at 0° C. The reaction temperature was raised to room temperature after 1 h. Stirred 2 h. Water (20 mL) was added and aqueous phase was extracted dichloromethane (2×30 mL). The combined organic phase was concentrated and purified by flash chromatography (eluent: dichloromethane). 1H nmr revealed the product was pure. Yield: 7.0 g, 96%

後処理

  1. temperatureThe reaction temperature was raised to room temperature after 1 h
  2. stirringStirred 2 h
  3. extractionaqueous phase was extracted dichloromethane (2×30 mL)
  4. concentrationThe combined organic phase was concentrated
  5. custompurified by flash chromatography (eluent: dichloromethane)

出典と根拠

ORDレコード
ord-18532b48adef474fa62a79baa547041c
出典データセット
uspto-grants-2014_09
特許番号
US08822548B2

関連ノート

読み込み中…