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Isopropanol → 2-Bromo-6-isopropoxypyridine

HRID 1641319
ノート
印刷プレビュー

反応式

HRID 1641319 の反応式
[CH:1]([OH:4])([CH3:3])[CH3:2].[Na].[Br:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9](Br)[N:8]=1>>[Br:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([O:4][CH:1]([CH3:3])[CH3:2])[N: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

4

反応物 3

HCID 3776IsopropanolHCID 122742,6-DibromopyridineHCID 5360545Sodium2 回

生成物 1

HCID 221807682-Bromo-6-isopropoxypyridine

反応条件

温度
80 °C

実験手順

The compound was prepared in a manner similar to that described in WO 02/076983 (page 80). Dry isopropanol (25 mL, 42.2 mmole) was placed in an oven-dried 250 ml 3 necked flask under nitrogen, sodium spheres (0.5 g, 21.1 mmol) were added and the reaction was heated to 80° C. to dissolve the sodium. 2,6 dibromopyridine (10 g, 42.2 mmole) was added as a solid and the reaction was heated at 95° C. After heating for ˜2.5 hr the reaction was cooled and partitioned between ether and water. The organic layer was evaporated to give a solid plus oil, the mixture was suspended in hexanes, cooled, and filtered to remove the solid. The filtrate was evaporated carefully and chromatographed on silica eluting with hexanes to give the product as a clear, colorless oil.

後処理

  1. customThe compound was prepared in a manner similar to
  2. additionwere added
  3. temperaturethe reaction was heated at 95° C
  4. temperatureAfter heating for ˜2.5 hr the reaction
  5. temperaturewas cooled
  6. custompartitioned between ether and water
  7. customThe organic layer was evaporated
  8. customto give a solid plus oil
  9. temperaturecooled
  10. filtrationfiltered
  11. customto remove the solid
  12. customThe filtrate was evaporated carefully
  13. customchromatographed on silica eluting with hexanes
  14. customto give the product as a clear, colorless oil

出典と根拠

ORDレコード
ord-e8cfb4d91af94cd18d3c56cc6cd6a1b1
出典データセット
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08114887B2

反応ノート

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