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(2-Methyl-4-nitrophenyl)methanol → 2-Methyl-4-nitrobenzaldehyde

HRID 2203297
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HRID 2203297 반응식
[CH3:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[CH2:11][OH:12]>[O-2].[Mn+4].[O-2].C(Cl)Cl>[CH3:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[CH:11]=[O:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 21345674(2-Methyl-4-nitrophenyl)methanol

생성물 1

HCID 126541462-Methyl-4-nitrobenzaldehyde수율 78.7%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 6344Dichloromethane용매

반응 조건

온도
40 °C

실험 절차

A flask was charged with (2-methyl-4-nitro-phenyl)-methanol (16.7 g, 0.100 mol) (334 mL), to manganese(IV) oxide (5 μm, 102.3 g, 1.00 mol), and CH2Cl2 (334 mL). The stirred mixture was heated at 40° C. for at least 2 h or until in-process HPLC analysis showed that conversion was greater than 95%. The cooled mixture was filtered through a celite cake (8 g) loaded onto a fritted funnel and the filter cake was rinsed with CH2Cl2 (340 mL). The filtrate and wash were concentrated under reduced pressure to dryness to afford the title compound as an amorphous solid (13.0 g, 78% yield).

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. filtrationThe cooled mixture was filtered through a celite cake (8 g)
  2. customloaded onto a fritted funnel
  3. washthe filter cake was rinsed with CH2Cl2 (340 mL)
  4. washThe filtrate and wash
  5. concentrationwere concentrated under reduced pressure to dryness

출처 및 근거

ORD 기록
ord-b900765e8dcd470fbd8412bf6cdb982a
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09365575B2

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