Hydrochloric Acid → Phenol, 4-[2-(4-nitrophenyl)ethenyl]-

HRID 6421

反応式

HRID 6421 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10](=[CH:14][C:15]2[CH:20]=[CH:19][C:18]([O:21]C(=O)C)=[CH:17][CH:16]=2)C(O)=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].C(O)C.Cl>O>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([CH:10]=[CH:14][C:15]2[CH:16]=[CH:17][C:18]([OH:21])=[CH:19][CH:20]=2)=[CH:8][CH:9]=1)([O-:3])=[O:2]

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 53778129alpha-p-Nitrophenyl-p-acetoxycinnamic Acid

生成物 1

HCID 139676Phenol, 4-[2-(4-nitrophenyl)ethenyl]-

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
95 °C

実験手順

A portion (36.75 grams) of a-p-nitrophenyl-p-acetoxycinnamic acid from A. above, ethanol (300 mL) and concentrated hydrochloric acid (300 mL) are added to a reactor equipped with a reflux condenser and stirred under a nitrogen atmosphere. Heating commenced and a reflux is achieved at 93° C. Refluxing continued over the next 262 minutes at which time the temperature has increased to 95° C. At this time, the contents of the reactor are poured into deionized water (one liter) and the resultant precipitate recovered by filtration. The wet filter cake is washed with two portions (500 mL) of deionized water then dissolved in stirred ethanol (750 mL) maintained at 82° C. The resultant solution is maintained at 4° C. for 15 hours. The precipitate is recovered by filtration and dried at 75° C. under a vacuum of 2 mm Hg to a constant weight of 22.70 grams of light orange colored crystalline needles. Fourier transform infrared spectrophotometric analysis of a potassium chloride pellet of a portion of the product revealed the presence of the expected hydroxyl group O--H stretching centered at 3422 cm-1 (broad), conjugated nitro group absorbances at 1516 and 1337 (1317 shoulder) cm-1 (sharp) and the ethylene C-H out-of-plane deformation at 972 cm-1.

後処理

  1. customequipped with a reflux condenser
  2. temperatureHeating
  3. customis achieved at 93° C
  4. temperatureRefluxing
  5. customcontinued over the next 262 minutes at which time
  6. filtrationthe resultant precipitate recovered by filtration
  7. washThe wet filter cake is washed with two portions (500 mL) of deionized water
  8. dissolutionthen dissolved in stirred ethanol (750 mL)
  9. temperaturemaintained at 82° C
  10. temperatureThe resultant solution is maintained at 4° C. for 15 hours
  11. filtrationThe precipitate is recovered by filtration
  12. dry with materialdried at 75° C. under a vacuum of 2 mm Hg to a constant weight of 22.70 grams of light orange colored crystalline needles

出典と根拠

ORDレコード
ord-bd2f92a102804b7a9cd611e6967e0025
出典データセット
uspto-grants-1993_09
特許番号
US05248758

関連ノート

読み込み中…