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Triacetoxyperiodinane → 2,2-Dimethyl-3-(3-methylcyclohexyl)propanal

HRID 2369786
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HRID 2369786 반응식
CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.[CH3:23][C:24]([CH3:35])([CH2:27][CH:28]1[CH2:33][CH2:32][CH2:31][CH:30]([CH3:34])[CH2:29]1)[CH2:25][OH:26]>ClCCl>[CH3:23][C:24]([CH3:35])([CH2:27][CH:28]1[CH2:33][CH2:32][CH2:31][CH:30]([CH3:34])[CH2:29]1)[CH:25]=[O:26]
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참가 물질

4

반응물 2

HCID 159087TriacetoxyperiodinaneHCID 574294222,2-Dimethyl-3-(3-methylcyclohexyl)propan-1-ol

생성물 1

HCID 574294212,2-Dimethyl-3-(3-methylcyclohexyl)propanal수율 33.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
0 °C

실험 절차

A solution of Dess Martin periodinane (9.0 g, 21.1 mmol, 1.3 eq) in dichloromethane (165 mL) was charged into a 250 mL three-necked round-bottom flask, equipped with a mechanical stirrer and a reflux condenser. The solution was cooled to 0° C. by the mean of an ice/salt bath. 2,2-dimethyl-3-(3-methylcyclohexyl)propan-1-ol (3.0 g, 16.3 mmol) was added dropwise. After stirring for 2 h at ambient temperature, the mixture was cooled down to −15° C. and the solid was filtered off. The organic solution was then concentrated. The resultant crude product was chromatographed on a silica gel column with 2% EtOAc in hexane as elution agent giving 2,2-dimethyl-3-(3-methylcyclohexyl)propanal (1.0 g, gc purity>85%; yield 33%).

후처리

  1. customequipped with a mechanical stirrer and a reflux condenser
  2. temperaturethe mixture was cooled down to −15° C.
  3. filtrationthe solid was filtered off
  4. concentrationThe organic solution was then concentrated
  5. customThe resultant crude product was chromatographed on a silica gel column with 2% EtOAc in hexane as elution agent

출처 및 근거

ORD 기록
ord-47e0ea507ee44889adeeed6b25d52564
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08709994B2

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