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Hydrazine hydrate (1:1) → 2-Hydrazinyl-6-methylpyridine

HRID 1529473
ノート
印刷プレビュー

反応式

HRID 1529473 の反応式
Br[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[N:3]=1.O.[NH2:10][NH2:11]>>[CH3:8][C:4]1[N:3]=[C:2]([NH:10][NH2:11])[CH:7]=[CH:6][CH:5]=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

3

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 792052-Bromo-6-methylpyridine

生成物 1

HCID 135904652-Hydrazinyl-6-methylpyridine

反応条件

温度
120 °C

実験手順

A mixture of 2-bromo-6-methyl-pyridine (602.10 g) and hydrazine hydrate (1570 ml) was refluxed at 120° C. for 6 hours, and then stirred at room temperature for about 48 hours. The solid separated was extracted with diethylether (3×1.5 L) and the combined ether extracts were washed with brine, dried over Na2SO4, filtered and concentrated (−430 g). The residue was stirred in a mixture of ether (200 ml) and hexane (1.5 L), filtered and washed with 5% diethylether in hexane to give a pale yellow solid (sticky). The solid was vacuum distilled at 106-113° C./2 mm, which solidified instantly. The solid was then dissolved in 2 L of diethylether and precipitated by adding 2 L of hexane, filtered and vacuum dried to give 1-(6-methylpyridin-2-yl)hydrazine as white solid (240 g).

後処理

  1. customThe solid separated
  2. extractionwas extracted with diethylether (3×1.5 L)
  3. washthe combined ether extracts were washed with brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated (−430 g)
  7. stirringThe residue was stirred in a mixture of ether (200 ml) and hexane (1.5 L)
  8. filtrationfiltered
  9. washwashed with 5% diethylether in hexane
  10. customto give a pale yellow solid (sticky)
  11. distillationdistilled at 106-113° C./2 mm, which
  12. dissolutionThe solid was then dissolved in 2 L of diethylether
  13. customprecipitated
  14. additionby adding 2 L of hexane
  15. filtrationfiltered
  16. customvacuum dried

出典と根拠

ORDレコード
ord-2be965c4070f4980b2506e455e1e0605
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09090625B2

反応ノート

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