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Bromine → 3-Bromo-5-chloro-2-methoxypyridine

HRID 280187
ノート
印刷プレビュー

反応式

HRID 280187 の反応式
C([O-])(=O)C.[Na+].[Cl:6][C:7]1[CH:8]=[CH:9][C:10]([O:13][CH3:14])=[N:11][CH:12]=1.[Br:15]Br>C(O)(=O)C>[Br:15][C:9]1[C:10]([O:13][CH3:14])=[N:11][CH:12]=[C:7]([Cl:6])[CH:8]=1
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

5

反応物 3

HCID 24408BromineHCID 517045Sodium AcetateHCID 47382765-Chloro-2-methoxypyridine

生成物 1

HCID 135677513-Bromo-5-chloro-2-methoxypyridine

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

反応条件

温度
80 °C

実験手順

To a stirred suspension of 2.5 g of anhydrous sodium acetate in 10 ml of acetic acid was added 4.3 g of 5-chloro-2-methoxypyridine followed by a solution of 3.1 ml of bromine in 10 ml of acetic acid. The mixture was warmed to 80° C. for 6 hours and then allowed to cool and stirred at 23° C. for 64 hours. It was then partitioned between ether and water and the resulting ether layer was washed with aqueous 1N sodium hydroxide solution and then with aqueous 5% sodium bisulfite solution, dried over potassium carbonate and concentrated at reduced pressure to leave a residual brown solid. This residue was bulb-to-bulb distilled with the material distilling at 140°-150° C. at 20 torr collected to give 3-bromo-5-chloro-2-methoxypyridine as a solid melting at about 45°-47.5° C.

後処理

  1. temperatureto cool
  2. customIt was then partitioned between ether and water
  3. washthe resulting ether layer was washed with aqueous 1N sodium hydroxide solution
  4. dry with materialwith aqueous 5% sodium bisulfite solution, dried over potassium carbonate
  5. concentrationconcentrated at reduced pressure
  6. customto leave a residual brown solid
  7. distillationdistilled with the material
  8. distillationdistilling at 140°-150° C. at 20 torr
  9. customcollected

出典と根拠

ORDレコード
ord-a57e399a64054ad68499af284a975daa
出典データセット
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04588733

反応ノート

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