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1,2,3-Trimethylbenzene → 2,3,4-trimethylbenzaldehyde

HRID 361295
ノート
印刷プレビュー

反応式

HRID 361295 の反応式
Cl[Sn](Cl)(Cl)Cl.ClC([O:9][CH3:10])Cl.[CH3:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([CH3:18])[C:13]=1[CH3:19]>ClCCl>[CH3:11][C:12]1[C:13]([CH3:19])=[C:14]([CH3:18])[CH:15]=[CH:16][C:17]=1[CH:10]=[O:9]
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

5

反応物 3

HCID 106861,2,3-TrimethylbenzeneHCID 21004Methane, dichloromethoxy-HCID 24287Tin tetrachloride

生成物 1

HCID 27525972,3,4-trimethylbenzaldehyde

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-5 °C

実験手順

To a stirred solution of SnCl4 (39 g, 0.15 mol) in 50 mL of dichloromethane was added dropwise at -5° C. a solution of 15 g (0.13 mol) of dichloromethylmethylether. This solution was stirred at -5° C. for one hour before adding dropwise over 10 min a solution of 12 g (0.1 mol) of 1,2,3-trimethylbenzene. The mixture was stirred at 0° C. for 15 min before warming to room temperature where it was stirred an additional 1.5 hrs. After quenching onto 100 g of ice the organic layer was separated, washed with water, saturated aqueous sodium bicarbonate and water before drying over Na2SO4, filtering and evaporating to dryness in vacuo. The product was purified by distillation in vacuo. B.p. 120°-122° C. (11 mm). Lit. b.p. 121.5 (11 mm) Yield: 9.2 g (70%).

後処理

  1. stirringThe mixture was stirred at 0° C. for 15 min
  2. temperaturebefore warming to room temperature where it
  3. stirringwas stirred an additional 1.5 hrs
  4. customAfter quenching onto 100 g of ice the organic layer
  5. customwas separated
  6. washwashed with water, saturated aqueous sodium bicarbonate and water
  7. dry with materialbefore drying over Na2SO4
  8. filtrationfiltering
  9. customevaporating to dryness in vacuo
  10. distillationThe product was purified by distillation in vacuo

出典と根拠

ORDレコード
ord-33a27399976e435da7c4122130599136
出典データセット
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05866513

反応ノート

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