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(3,4,5-Trimethoxy-2-nitrophenyl)methanol → 3,4,5-Trimethoxy-2-nitrobenzaldehyde

HRID 2289575
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HRID 2289575 반응식
[CH3:1][O:2][C:3]1[C:4]([N+:15]([O-:17])=[O:16])=[C:5]([CH:8]=[C:9]([O:13][CH3:14])[C:10]=1[O:11][CH3:12])[CH2:6][OH:7]>C(Cl)Cl.[O-2].[O-2].[Mn+4]>[CH3:1][O:2][C:3]1[C:4]([N+:15]([O-:17])=[O:16])=[C:5]([CH:8]=[C:9]([O:13][CH3:14])[C:10]=1[O:11][CH3:12])[CH:6]=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 227988(3,4,5-Trimethoxy-2-nitrophenyl)methanol

생성물 1

HCID 186979183,4,5-Trimethoxy-2-nitrobenzaldehyde수율 30%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매2회HCID 6344Dichloromethane용매

실험 절차

Active manganese dioxide (8.0 g) was added to a solution of 3,4,5-trimethoxy-2-nitrobenzyl alcohol (1.01 g, 4.15 mmol), prepared in the step (a), in methylene chloride (15 ml), and the mixture was stirred at room temperature overnight. Further, active manganese dioxide (8.0 g) was added thereto, and the mixture was stirred at room temperature for 8 hr. The reaction mixture was filtered through Celite, and the solvent was removed under reduced pressure to give 3,4,5-trimethoxy-2-nitrobenzaldehyde (300 mg, 30%) as colorless powder.

후처리

  1. stirringthe mixture was stirred at room temperature for 8 hr
  2. filtrationThe reaction mixture was filtered through Celite
  3. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-ef5325f9ec414c1bb60e57b17cff8077
출처 데이터셋
uspto-grants-2000_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06093714

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