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Nitric Acid → 4-Cyclohexyl-2-nitrophenol

HRID 1723009
ノート
印刷プレビュー

反応式

HRID 1723009 の反応式
CCOCC.[CH:6]1([C:12]2[CH:17]=[CH:16][C:15]([OH:18])=[CH:14][CH:13]=2)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.[N+:19]([O-])([OH:21])=[O:20]>O>[CH:6]1([C:12]2[CH:13]=[CH:14][C:15]([OH:18])=[C:16]([N+:19]([O-:21])=[O:20])[CH:17]=2)[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11]1
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 944Nitric AcidHCID 3283Diethyl EtherHCID 143274-Cyclohexylphenol

生成物 1

HCID 150363164-Cyclohexyl-2-nitrophenol

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

To a stirred mixture of 50 ml of water, 50 ml of ether and 10.0 g of 4-cyclohexylphenol, was added dropwise 12.6 ml of 60% nitric acid while cooling with ice. The temperature of the mixture was raised to room temperature and the reaction was carried out for a day. After 500 ml of water was added, the reaction mixture was extracted with 500 ml of ethyl acetate, washed with water and a brine successively and dried with anhydrous sodium sulfate. The drying agent was filtered off and the solvent was distilled away. The residue was purified by subjecting to silica-gel column-chromatography [eluent:chloroform] to give 6.92 g of 4-cyclohexyl-2-nitrophenol.

後処理

  1. temperaturewhile cooling with ice
  2. waitthe reaction was carried out for a day
  3. extractionthe reaction mixture was extracted with 500 ml of ethyl acetate
  4. washwashed with water
  5. dry with materiala brine successively and dried with anhydrous sodium sulfate
  6. filtrationThe drying agent was filtered off
  7. distillationthe solvent was distilled away
  8. customThe residue was purified

出典と根拠

ORDレコード
ord-44f9c95b880548f2acd2cc9e4e80a416
出典データセット
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04859661

反応ノート

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