m-Chloroperbenzoic acid → 3-Bromo-5-fluoro-2,4-dimethylpyridine 1-oxide

HRID 1502464ノート

反応式

HRID 1502464 の反応式
[Br:1][C:2]1[C:3]([CH3:10])=[N:4][CH:5]=[C:6]([F:9])[C:7]=1[CH3:8].ClC1C=C(C=CC=1)C(OO)=[O:16]>ClCCl>[Br:1][C:2]1[C:3]([CH3:10])=[N+:4]([O-:16])[CH:5]=[C:6]([F:9])[C:7]=1[CH3:8]

参加物

4

反応物 2

HCID 70297m-Chloroperbenzoic acidHCID 679747603-Bromo-5-fluoro-2,4-dimethylpyridine

生成物 1

HCID 679750773-Bromo-5-fluoro-2,4-dimethylpyridine 1-oxide収率 93%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A mixture of 3-bromo-5-fluoro-2,4-dimethyl-pyridine (220 mg, 1.08 mmol) and 3-chloroperoxybenzoic acid (399 mg, 1.62 mmol) in dichloromethane (3 mL) was stirred overnight at room temperature. The reaction mixture was diluted with DCM (50 mL) and washed with saturated aqueous sodium thiosulfite (10 mL) followed by saturated aqueous sodium bicarbonate (10 mL). The organic layer was separated, dried over sodium sulfate, filtered and concentrated in vacuo to provide a residue that was purified by flash chromatography (4 g, Silica, 0-10% methanol in DCM). Desired fractions were combined and evaporated in vacuo to afford the title compound as a white solid (220 mg, 93%), which was used in the next step without further purification.

後処理

  1. washwashed with saturated aqueous sodium thiosulfite (10 mL)
  2. customThe organic layer was separated
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customto provide a residue that
  7. customwas purified by flash chromatography (4 g, Silica, 0-10% methanol in DCM)
  8. customevaporated in vacuo

出典と根拠

ORDレコード
ord-17e64470f9b34f5ea618e5f53067b71b
出典データセット
uspto-grants-2015_12
特許番号
US09206175B2

反応ノート

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