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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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(2-Methyl-4-nitrophenyl)methanol → 2-Methyl-4-nitrobenzaldehyde

HRID 2203297
ノート
印刷プレビュー

反応式

HRID 2203297 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

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

生成物 1

HCID 126541462-Methyl-4-nitrobenzaldehyde収率 78.7%

試薬・触媒・溶媒 2

HCID 178418406HCID 178418406、化合物触媒HCID 6344Dichloromethane溶媒

反応条件

温度
40 °C

実験手順

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).

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  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

出典と根拠

ORDレコード
ord-b900765e8dcd470fbd8412bf6cdb982a
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09365575B2

反応ノート

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