Hydrazine hydrate (1:1) → 5-(4-Chloro-phenyl)-2,4-dihydro-pyrazol-3-one
反応式
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([C:6]([C:8](C)(C)[C:9](OCC)=[O:10])=O)=[CH:4][CH:3]=1.O.[NH2:19][NH2:20]>C(O)C>[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([C:6]2[CH2:8][C:9](=[O:10])[NH:20][N:19]=2)=[CH:4][CH:3]=1参加物
4
実験手順
A mixture of 26 g (0.10 mmol) of ethyl α-(4-chlorobenzoyl)isobutyrate, 10 g (0.20 mmol) of hydrazine monohydrate and 200 ml of ethanol was heated under reflux for 18 hours. The reaction solution was concentrated under reduced pressure. The obtained crude product was washed successively with water, methanol-water and diethyl ether-n-hexane, and then air dried to give 16 g of the object compound as white crystals (yield 84%).
後処理
- temperaturewas heated
- temperatureunder reflux for 18 hours
- concentrationThe reaction solution was concentrated under reduced pressure
- customThe obtained crude product
- washwas washed successively with water, methanol-water and diethyl ether-n-hexane
- customair dried
出典と根拠
- ORDレコード
- ord-5449332995294ab599caac6f51e011c8
- 出典データセット
- uspto-grants-1997_06
- 特許番号
- US05639776
反応ノート
読み込み中…