反応式
O.O=[C:3]([C:7]([OH:9])=[O:8])[C:4]([OH:6])=[O:5].[C:10]1([NH:16][NH2:17])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>C(O)C.O>[C:10]1([NH:16][N:17]=[C:3]([C:7]([OH:9])=[O:8])[C:4]([OH:6])=[O:5])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1参加物
5
実験手順
To a vigorously stirred solution of ketomalonic acid monohydrate (29.33 g) in ethanol (140 ml) and water (300 ml) at ambient temperature was added phenylhydrazine (23.3 g) dropwise over a 40 minute period. The resultant slurry was stirred overnight at ambient temperature. The solid was separated by filtration, washed sucessively with cold water (100 ml) and ethanol (25 ml) and air dried. Subsequent drying was performed at 75° C. overnight in a vacuum oven to give the title compound as a yellow solid (42.38 g). 1H (300 MHz, DMSO-d6): d 7.12(t, 1H), 7.35-7.48(m, 4H); m.p.: 155-157° C. (dec).
後処理
- customThe solid was separated by filtration
- washwashed sucessively with cold water (100 ml) and ethanol (25 ml) and air
- customdried
- customSubsequent drying
- waitwas performed at 75° C. overnight in a vacuum oven
出典と根拠
- ORDレコード
- ord-f5a07a0fb14e4af69cbcf50d1e4bc63c
- 出典データセット
- uspto-grants-1999_06
- 特許番号
- US05910495
関連ノート
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