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O-Cresol → 3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro2-naphthol

HRID 1384161
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HRID 1384161 반응식
Cl[C:2]([CH3:10])([CH2:4][CH2:5][C:6](Cl)([CH3:8])[CH3:7])[CH3:3].[CH3:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[OH:18].[Cl-].[Al+3].[Cl-].[Cl-]>ClCCl>[CH3:11][C:12]1[C:13]([OH:18])=[CH:14][C:15]2[C:2]([CH3:10])([CH3:3])[CH2:4][CH2:5][C:6]([CH3:8])([CH3:7])[C:16]=2[CH:17]=1
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참가 물질

5

반응물 3

HCID 335O-CresolHCID 80360Hexane, 2,5-dichloro-2,5-dimethyl-HCID 6451240Aluminum(III) Chloride

생성물 1

HCID 2266903,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro2-naphthol

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

50.8 g (0.27 mol) of 2,5-dichloro-2,5-dimethylhexane, 30 g (0.27 mol) of 2-methylphenol and 500 ml of dichloromethane are introduced into a three-necked flask. 14.8 g (0.11 mol) of aluminium chloride are added portionwise, at 0° C., and the mixture is stirred at room temperature for twelve hours. The reaction medium is poured into ice-cold water, the mixture is extracted with dichloromethane and the organic phase is separated out after settling has taken place, washed with bicarbonate solution, dried over magnesium sulphate and evaporated. The residue obtained is triturated in hexane and filtered off and, after drying, 54.4 g (90%) of the expected phenol, with a melting point of 125-6° C., are collected.

후처리

  1. additionThe reaction medium is poured into ice-cold water
  2. extractionthe mixture is extracted with dichloromethane
  3. customthe organic phase is separated out after settling
  4. washwashed with bicarbonate solution
  5. dry with materialdried over magnesium sulphate
  6. customevaporated
  7. customThe residue obtained
  8. customis triturated in hexane
  9. filtrationfiltered off
  10. customafter drying
  11. custom54.4 g (90%) of the expected phenol, with a melting point of 125-6° C., are collected

출처 및 근거

ORD 기록
ord-2d35c697c07d4d3fb9331b577bdce734
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06258775B1

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