Benzyl Alcohol → 2-Benzyloxy-6-bromopyridine

HRID 356823

反応式

HRID 356823 の反応式
[CH2:1]([OH:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].[Br:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14](Br)[N:13]=1>CN(C)C=O>[Br:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[N:13]=1

参加物

5

反応物 3

HCID 244Benzyl AlcoholHCID 122742,6-DibromopyridineHCID 24758Sodium hydride

生成物 1

HCID 8174752-Benzyloxy-6-bromopyridine

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

2.9 ml benzyl alcohol was dissolved in 10 ml N,N-dimethylformamide and 0.7 g sodium hydride (purity 95%) was slowly added. After gas evolution has ceased, 6 g 2,6-dibromopyridine was added and the mixture heated to reflux for 3 hours. After cooling, the reaction mixture was filtered through a silica gel column using hexane/ethyl acetate 1/1. The solvent was removed in vacuo and the crude product purified by flash silica gel column chromatography. The title compound was obtained as a colourless oil.

後処理

  1. temperaturethe mixture heated
  2. temperatureto reflux for 3 hours
  3. temperatureAfter cooling
  4. filtrationthe reaction mixture was filtered through a silica gel column
  5. customThe solvent was removed in vacuo
  6. customthe crude product purified by flash silica gel column chromatography

出典と根拠

ORDレコード
ord-dd8a0f9c73de4234a94252a5f2a542a8
出典データセット
uspto-grants-1998_11
特許番号
US05840654

関連ノート

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