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N-(4-Chloro-3-hydroxymethyl-benzyl)-propionamide → N-(4-chloro-3-formylbenzyl)propionamide

HRID 2428132
ノート
印刷プレビュー

反応式

HRID 2428132 の反応式
[Cl:1][C:2]1[CH:13]=[CH:12][C:5]([CH2:6][NH:7][C:8](=[O:11])[CH2:9][CH3:10])=[CH:4][C:3]=1[CH2:14][OH:15]>CC#N.O=[Mn]=O>[Cl:1][C:2]1[CH:13]=[CH:12][C:5]([CH2:6][NH:7][C:8](=[O:11])[CH2:9][CH3:10])=[CH:4][C:3]=1[CH:14]=[O:15]
参加物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 67148202N-(4-Chloro-3-hydroxymethyl-benzyl)-propionamide

生成物 1

HCID 86632361N-(4-chloro-3-formylbenzyl)propionamide収率 93%

試薬・触媒・溶媒 2

HCID 14801Manganese dioxide触媒2 回HCID 6342Acetonitrile溶媒

実験手順

MnO2 (5.61 g, 65.7 mmol) was added to a sol. of N-(4-chloro-3-hydroxymethyl-benzyl)-propionamide (2.99 g, 13.1 mmol) in CH3CN (255 mL) at rt. The mixture was stirred for 3 h at rt, and MnO2 (2.24 g, 26.2 mmol) was added again. The mixture was stirred for 1 h at rt, and the mixture was filtered through celite. The filtrate was evaporated under reduced pressure, and the residue was dried under high vacuum to yield the crude title compound (2.74 g, 93%) that was used further without purification. LC-MS: tR=0.76 min; ES+: 267.27.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. stirringThe mixture was stirred for 1 h at rt
  2. filtrationthe mixture was filtered through celite
  3. customThe filtrate was evaporated under reduced pressure
  4. customthe residue was dried under high vacuum

出典と根拠

ORDレコード
ord-a0eaa42206434cfcbb4ec045294a6af7
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07968720B2

反応ノート

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