Triethanolamine → 1-Ethenyl-4-nitrobenzene

HRID 1982475

反応式

HRID 1982475 の反応式
[N+:1]([C:4]1[CH:12]=[CH:11][C:7]([CH2:8][CH2:9]Br)=[CH:6][CH:5]=1)([O-:3])=[O:2].N(CCO)(CCO)CCO>O>[N+:1]([C:4]1[CH:12]=[CH:11][C:7]([CH:8]=[CH2:9])=[CH:6][CH:5]=1)([O-:3])=[O:2]

参加物

4

実験手順

A 500 ml 3-neck round bottom flask was fitted with a thermometer and steam distillation apparatus. The flask was charged with 12.5 g (0.054 mol) of 4-nitrophenethyl bromide, 75 ml (0.565 mol) of triethanolamine and 50 ml of water. The reaction mixture was heated to reflux and the mixture was allowed to slowly steam distill. Approximately 100 mg of hydroquinone was added to the distillate collected in order to prevent polymerization. The distillate was extracted three times with diethyl ether and the combined organic phases were washed with water, 1N hydrochloric acid, water, and a saturated sodium chloride solution in sequence. The organic phase was dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure to provide 7.193 g of 4-nitrostyrene as an oil which solidified upon cooling. Additional quantities of this material were prepared by the general procedure above.

後処理

  1. customA 500 ml 3-neck round bottom flask was fitted with a thermometer and steam distillation apparatus
  2. temperatureThe reaction mixture was heated
  3. temperatureto reflux
  4. distillationdistill
  5. additionApproximately 100 mg of hydroquinone was added to the distillate
  6. customcollected in order
  7. custompolymerization
  8. extractionThe distillate was extracted three times with diethyl ether
  9. washthe combined organic phases were washed with water, 1N hydrochloric acid, water
  10. dry with materialThe organic phase was dried over anhydrous sodium sulfate
  11. customevaporated to dryness under reduced pressure

出典と根拠

ORDレコード
ord-786fb782a4de42d6b26a5a443924864f
出典データセット
uspto-grants-1986_06
特許番号
US04596827

関連ノート

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