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HCID 57682805, 화합물 → HCID 57682838, 화합물

HRID 494984
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HRID 494984 반응식
[CH3:1][C:2]1([CH3:21])[O:6][CH:5]([CH2:7][C:8]2[C:13]([O:14][CH3:15])=[CH:12][C:11]([CH2:16][OH:17])=[C:10]([N+:18]([O-:20])=[O:19])[CH:9]=2)[CH2:4][O:3]1>C(Cl)Cl.[O-2].[O-2].[Mn+4]>[CH3:1][C:2]1([CH3:21])[O:6][CH:5]([CH2:7][C:8]2[C:13]([O:14][CH3:15])=[CH:12][C:11]([CH:16]=[O:17])=[C:10]([N+:18]([O-:20])=[O:19])[CH:9]=2)[CH2:4][O:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 57682805HCID 57682805, 화합물

생성물 1

HCID 57682838HCID 57682838, 화합물수율 54.5%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 6344Dichloromethane용매

실험 절차

Thereafter, 253 mg of (4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-5-methoxy-2-nitrophenyl)methanol was dissolved in 10 ml of methylene chloride. Then, 2.5 g of activated manganese dioxide was added to the reaction solution, and the obtained mixture was then stirred at room temperature for 66 hours. Thereafter, the reaction solution was filtered through celite, and the filtrate was concentrated under a reduced pressure, so as to obtain 137 mg of the subject compound.

후처리

  1. filtrationThereafter, the reaction solution was filtered through celite
  2. concentrationthe filtrate was concentrated under a reduced pressure

출처 및 근거

ORD 기록
ord-cef346a764064d3694f2bbf70c053e27
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07538123B2

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