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Epichlorohydrin → HCID 22386937、化合物

HRID 1072498
ノート
印刷プレビュー

反応式

HRID 1072498 の反応式
[CH3:1][C:2]1[C:3]([NH:9][C:10](=[O:12])[CH3:11])=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.[CH2:13]([CH:15]1[O:17][CH2:16]1)Cl.[OH-].[Na+].CCOC(C)=O>[Cl-].C([N+](CC)(CC)CC1C=CC=CC=1)C.CCCCCCC>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8][CH2:13][CH:15]2[CH2:16][O:17]2)[C:3]=1[NH:9][C:10](=[O:12])[CH3:11]
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

7

反応物 4

HCID 7835EpichlorohydrinHCID 8857Ethyl AcetateHCID 14798Sodium HydroxideHCID 153835Acetamide, N-(2-hydroxy-6-methylphenyl)-

生成物 1

HCID 22386937HCID 22386937、化合物

試薬・触媒・溶媒 2

HCID 66133Benzyl triethylammonium chloride触媒
HCID 8900
Heptane
溶媒

反応条件

温度
70 °C

実験手順

A mixture of 3-methyl-2-acetamidophenol (0.165 g, 1 mmol), and epichlorohydrin (1.84 g, 20 mmol) was stirred at 70° C. to afford a clear solution. Triethylbenzylammonium chloride (0.15 g, 1 mmol) was then added and stirring was continued at 125° C. for 15 minutes. After cooling to room temperature 1M NaOH solution was added and the solution was extracted with dichloromethane. The organic extract was washed with water and dried. After evaporation of the dichloromethane the resulting brownish oil was purified through silica chromatography 50-70% EtOAc in heptane yielding the product as a colourless oil (0.12 g, 0.54 mmol).

後処理

  1. customto afford a clear solution
  2. stirringstirring
  3. additionwas added
  4. extractionthe solution was extracted with dichloromethane
  5. extractionThe organic extract
  6. washwas washed with water
  7. customdried
  8. customAfter evaporation of the dichloromethane the resulting brownish oil

出典と根拠

ORDレコード
ord-4039b81384b84092a46a7cfccebd5b38
出典データセット
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06911458B2

反応ノート

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