Hydrazine hydrate (1:1) → 4-Phenylpyridazine-3,6-diol

HRID 1425727ノート

反応式

HRID 1425727 の反応式
[C:1]1([C:7]2[C:8](=O)[O:9][C:10](=[O:12])[CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.O.[NH2:15][NH2:16]>C(O)C>[C:1]1([C:7]2[C:8](=[O:9])[NH:15][NH:16][C:10](=[O:12])[CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

参加物

4

実験手順

4.0 g (23 mmole) of 3-phenylfuran-2,5-dione was added to a 100 ml single-necked round bottom flask followed by 2.9 g (27.6 mmole) of hydrazine monohydrate and then 20 ml of reagent grade ethanol (95%). The flask was fitted with a reflux condenser and the reaction mixture was heated to reflux in an oil bath at 110 degree (temperature of oil bath) and stirred for 2 h. The flask was then removed from the oil bath and the reaction mixture cooled to ambient temperature. The stir bar was removed and the solvent was evaporated in vacuo in a water bath at 45 degree. The residue was then treated with 50 ml of Milli-Q water and stirred for 10 minutes to give a suspension. The precipitate was collected by filtering, washed with 100 ml of Milli-Q water, and dried over a medium frit sintered glass funnel in vacuo to give 3.9 g of white solid. Yield, 91%, confirmed by ESI-MS. ESI-MS: m/z 189.2 (M+H+).

後処理

  1. customThe flask was fitted with a reflux condenser
  2. temperaturethe reaction mixture was heated
  3. temperatureto reflux in an oil bath at 110 degree (temperature of oil bath)
  4. customThe flask was then removed from the oil bath
  5. customThe stir bar was removed
  6. customthe solvent was evaporated in vacuo in a water bath at 45 degree
  7. additionThe residue was then treated with 50 ml of Milli-Q water
  8. stirringstirred for 10 minutes
  9. customto give a suspension
  10. customThe precipitate was collected
  11. filtrationby filtering
  12. washwashed with 100 ml of Milli-Q water
  13. customdried over a medium frit sintered glass funnel in vacuo

出典と根拠

ORDレコード
ord-17cd455e92114fb0aff720060ebad595
出典データセット
uspto-grants-2015_01
特許番号
US08933076B2

反応ノート

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