(5-Bromo-3-pyridinyl)methanol → 5-Bromo-3-pyridinecarboxaldehyde

HRID 30469

反応式

HRID 30469 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH2:8][OH:9])[CH:5]=[N:6][CH:7]=1>O=[Mn]=O>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[O:9])[CH:5]=[N:6][CH:7]=1

参加物

3

反応物 1

HCID 2784733(5-Bromo-3-pyridinyl)methanol

生成物 1

HCID 27847345-Bromo-3-pyridinecarboxaldehyde収率 51.1%

試薬・触媒・溶媒 1

HCID 14801Manganese dioxide触媒

実験手順

(5-Bromo-pyridin-3-yl)-methanol (1.13 g, 6.00 mmol) was dissolved in CHCI3 (40 mL) and treated with MnO2 (3.60 g). The reaction mixture was heated at reflux temperature for 3 h. The hot reaction mixture was filtered through a pad of diatomaceous earth and the filtrate was concentrated to yield the title compound (0.570 g, 51%).

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux temperature for 3 h
  3. filtrationThe hot reaction mixture was filtered through a pad of diatomaceous earth
  4. concentrationthe filtrate was concentrated

出典と根拠

ORDレコード
ord-a363896c2f4243088d27486a0d5c3e7a
出典データセット
uspto-grants-2008_09
特許番号
US07423147B2

関連ノート

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