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Nitric Acid → 4-Cyclohexyl-2-nitrophenol

HRID 1723009
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반응식

HRID 1723009 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 944Nitric AcidHCID 3283Diethyl EtherHCID 143274-Cyclohexylphenol

생성물 1

HCID 150363164-Cyclohexyl-2-nitrophenol

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-44f9c95b880548f2acd2cc9e4e80a416
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04859661

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