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Hydrochloric Acid → HCID 178447948、化合物

HRID 1250129
ノート
印刷プレビュー

反応式

HRID 1250129 の反応式
[CH2:1]([C@H:4]1[CH2:9][CH2:8][C@H:7]([CH:10]=[CH:11][C:12]2[CH:19]=[CH:18][C:15]([C:16]#[N:17])=[CH:14][CH:13]=2)[CH2:6][CH2:5]1)[CH2:2][CH3:3].Cl.C(O)C>O>[CH2:1]([C@H:4]1[CH2:5][CH2:6][C@H:7](/[CH:10]=[CH:11]/[C:12]2[CH:19]=[CH:18][C:15]([C:16]#[N:17])=[CH:14][CH:13]=2)[CH2:8][CH2:9]1)[CH2:2][CH3:3]
参加物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 313Hydrochloric AcidHCID 702EthanolHCID 178447949HCID 178447949、化合物

生成物 1

HCID 178447948HCID 178447948、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

This nitrile in an amount of 11.7 g (0.05 ml) was added to a mixture of 13.9 g (0.07 ml) of dihydrated sodium benzenesufinate, 12 ml of 6N-HCl, and 70 ml of ethanol, and reacted under reflux for 4 hours. After finishing of the reaction, 50 ml of water was added to the reaction product and then extracted with 150 ml of toluene. The organic layer thus obtained was washed with saturated aqueous sodium carbonate solution thrice and with water thrice, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under a reduced pressure, and the residue was subjected to silica gel column chromatography (eluent: toluene) to obtain 12.0 g of a crude (E)-4-(2-(trans-4-propylcyclohexyl)vinyl)benzonitrile.

後処理

  1. customreacted
  2. temperatureunder reflux for 4 hours
  3. additionwas added to the reaction product
  4. extractionextracted with 150 ml of toluene
  5. customThe organic layer thus obtained
  6. washwas washed with saturated aqueous sodium carbonate solution thrice and with water thrice
  7. dry with materialdried over anhydrous magnesium sulfate
  8. distillationThe solvent was distilled off under a reduced pressure

出典と根拠

ORDレコード
ord-8401e86d5df94a54a6afd24d120253dd
出典データセット
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06337034B1

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート