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Diethyl Ether → Cyclohexanone, 2-(2-methylphenyl)-

HRID 2218558
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HRID 2218558 반응식
[C:1]1([CH3:14])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH:7]1[CH2:12][CH2:11][CH2:10][CH2:9][CH:8]1[OH:13].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.C(OCC)C>ClCCl>[C:1]1([CH3:14])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH:7]1[CH2:12][CH2:11][CH2:10][CH2:9][C:8]1=[O:13]
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참가 물질

5

반응물 3

HCID 3283Diethyl Ether2회HCID 159087TriacetoxyperiodinaneHCID 2513132-(o-Tolyl)cyclohexanol

생성물 1

HCID 3048041Cyclohexanone, 2-(2-methylphenyl)-수율 54.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To (cis/trans) 2-o-tolyl-cyclohexanol (1 g) in dichloromethane (30 ml) was added Dess-Martin periodinane (Aldrich 27,462-3) at room temperature. The reaction mixture was allowed to stir at room temperature for 16 hours before diethyl ether was added. The volume of solvent was reduced in vacuo to about one quarter of the initial amount. More diethylether (87 ml) was added and the solution was washed with a 10% solution of sodium thiosulfate (87 ml), a solution of saturated sodium bicarbonate (87 ml), brine (100 mL) and water (100 ml). The organic phase was then dried over sodium sulfate and concentrated in vacuo. The residue was then purified by column chromatography to give 0.54 g of 2-o-tolyl-cyclohexanone MS (EI) 188.2 (M+).

후처리

  1. additionwas added
  2. washthe solution was washed with a 10% solution of sodium thiosulfate (87 ml)
  3. dry with materialThe organic phase was then dried over sodium sulfate
  4. concentrationconcentrated in vacuo
  5. customThe residue was then purified by column chromatography

출처 및 근거

ORD 기록
ord-647fccf5f7c94a3897c582ba380fba0b
출처 데이터셋
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07411093B2

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