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2-Methoxy-3-hydroxymethyl-5-ethyl-6-methylpyridine → 2-Methoxy-5-ethyl-6-methylnicotinaldehyde

HRID 273681
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인쇄 미리보기

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HRID 273681 반응식
[CH3:1][O:2][C:3]1[C:8]([CH2:9][OH:10])=[CH:7][C:6]([CH2:11][CH3:12])=[C:5]([CH3:13])[N:4]=1>C1C=CC=CC=1.[O-2].[O-2].[Mn+4]>[CH3:1][O:2][C:3]1[N:4]=[C:5]([CH3:13])[C:6]([CH2:11][CH3:12])=[CH:7][C:8]=1[CH:9]=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 152284142-Methoxy-3-hydroxymethyl-5-ethyl-6-methylpyridine

생성물 1

HCID 102616792-Methoxy-5-ethyl-6-methylnicotinaldehyde수율 90.1%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 241Benzene용매

실험 절차

Activated manganese dioxide (2.0 g) was added to a solution of 2-methoxy-3-hydroxymethyl-5-ethyl-6-methylpyridine (1.18 g, 6.5 mmol) in dry benzene (20 mL) and refluxed 5-10 hours. The warm suspension was filtered through a pad of anhydrous Na2SO4 and evaporated to yield 1.05 g (90%) of a viscous oil which solidified.

후처리

  1. temperaturerefluxed 5-10 hours
  2. filtrationThe warm suspension was filtered through a pad of anhydrous Na2SO4
  3. customevaporated

출처 및 근거

ORD 기록
ord-d2bbc18a1e6b40b2ae6c5fe1e46175bf
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05387512

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