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Hydrazine hydrate (1:1) → 1,4-Dibenzylbenzene

HRID 613586
ノート
印刷プレビュー

反応式

HRID 613586 の反応式
[C:1]([C:9]1[CH:14]=[CH:13][C:12]([C:15](=O)[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[CH:11][CH:10]=1)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O.NN>C(O)COCCO>[CH2:15]([C:12]1[CH:13]=[CH:14][C:9]([CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:10][CH:11]=1)[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1
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

4

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 763951,4-Dibenzoylbenzene

生成物 1

HCID 2360471,4-Dibenzylbenzene収率 97.4%

試薬・触媒・溶媒 1

HCID 8117Diethylene Glycol溶媒

反応条件

温度
100 °C

実験手順

In a 4 neck, 1 liter flask fitted with thermocouple, mechanical stirrer, Barrett trap with condenser, nitrogen line, and stopper, was added 1,4-dibenzoylbenzene (90.5 g), hydrazine monohydrate (172.4 g) and diethyleneglycol (400 ml). The reaction mixture was heated at 100° C. for 1.5 hours. The mixture was then heated to 150° C. while collecting water and excess hydrazine hydrate in the Barrett trap. Potassium hydroxide (54.1 g) was slowly added over 0.5 hour while the temperature was slowly increased to 200° C. The temperature was maintained at 200° C. for 1 hour. The reaction was cooled to 80° C. and then poured into 500 ml water. The reactor was rinsed with an additional 550 ml water and combined with the quench solution. The water was extracted 3 times with 250 ml dichloromethane, the combined organic phases were washed with 500 ml water, dried over magnesium sulfate, filtered and the solvent removed on a rotary evaporator to give 1,4-dibenzylbenzene as a white solid (79.5 g, 97.4% yield).

後処理

  1. customIn a 4 neck, 1 liter flask fitted with thermocouple, mechanical stirrer, Barrett trap with condenser
  2. temperatureThe mixture was then heated to 150° C.
  3. customwhile collecting water and excess hydrazine hydrate in the Barrett trap
  4. additionPotassium hydroxide (54.1 g) was slowly added over 0.5 hour while the temperature
  5. temperaturewas slowly increased to 200° C
  6. temperatureThe temperature was maintained at 200° C. for 1 hour
  7. temperatureThe reaction was cooled to 80° C.
  8. additionpoured into 500 ml water
  9. washThe reactor was rinsed with an additional 550 ml water
  10. extractionThe water was extracted 3 times with 250 ml dichloromethane
  11. washthe combined organic phases were washed with 500 ml water
  12. dry with materialdried over magnesium sulfate
  13. filtrationfiltered
  14. customthe solvent removed on a rotary evaporator

出典と根拠

ORDレコード
ord-895b1b71e6444cdba1a0efd723905ae1
出典データセット
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06008283

反応ノート

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