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Sodium Bicarbonate → 6-Acetoxy-2-formylbicyclo[3,3,0]octane

HRID 462789
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HRID 462789 반응식
[C:1]([O:4][CH:5]1[CH2:12][CH2:11][CH:10]2[CH:6]1[CH2:7][CH2:8][CH:9]2[CH2:13][OH:14])(=[O:3])[CH3:2].[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1.C(=O)(O)[O-].[Na+]>ClCCl>[C:1]([O:4][CH:5]1[CH2:12][CH2:11][CH:10]2[CH:6]1[CH2:7][CH2:8][CH:9]2[CH:13]=[O:14])(=[O:3])[CH3:2]
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참가 물질

5

반응물 3

HCID 516892Sodium BicarbonateHCID 203972176-Acetoxy-2-hydroxymethylbicyclo[3,3,0]octaneHCID 178418287HCID 178418287, 화합물

생성물 1

HCID 203971916-Acetoxy-2-formylbicyclo[3,3,0]octane

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A stirred solution of 6-acetoxy-2-hydroxymethylbicyclo[3,3,0]octane (0.10 g; prepared as described in Reference Example 20 and predominantly in the 2β-configuration) in dry dichloromethane (2.5 ml) was treated with pyridinium chlorochromate (0.22 g) and anhydrous sodium bicarbonate (0.083 g). The resulting suspension was stirred for 150 minutes at the ambient temperature and was then placed directly onto a short column of silica gel and subjected to medium pressure, short column chromatography, eluting with a mixture of ethyl acetate and toluene (1:1 v/v) to give 6-acetoxy-2-formylbicyclo[3,3,0]octane (0.070 g), predominantly in the 2β-configuration.

후처리

  1. customprepared
  2. washeluting with a mixture of ethyl acetate and toluene (1:1 v/v)

출처 및 근거

ORD 기록
ord-2b5115520080487b99b24e50dd863a8a
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04517202

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