Water → 4-[(2,4-Dichlorophenyl)phenylmethyl]-1H-pyrazole
反応式
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH:9]([CH:16]([CH:19]=O)[CH:17]=O)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[NH2:21][NH2:22].O>C(O)C>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH:9]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:16]1[CH:19]=[N:21][NH:22][CH:17]=1参加物
5
実験手順
Two grams of [(2,4-dichlorophenyl)phenylmethyl]malonaldehyde in 10 ml of ethanol were heated with 3 ml of anhydrous hydrazine on a steam bath for two hours. The reaction mixture was poured into water and extracted with ether. The ether extract was dried, filtered, and evaporated. The residue was crystallized twice from Skelley B/acetone to provide 1.2 g of the desired title product, m.p. 131° C.
後処理
- extractionextracted with ether
- extractionThe ether extract
- customwas dried
- filtrationfiltered
- customevaporated
- customThe residue was crystallized twice from Skelley B/acetone
出典と根拠
- ORDレコード
- ord-cb337b6c2bb44925af26f18ccc8fd109
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04609666
反応ノート
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