Sodium Hydroxide → N-[4-(2-chlorophenyl)but-3-en-2-ylidene]hydroxylamine
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1/[CH:8]=[CH:9]/[C:10](=O)[CH3:11].Cl.[NH2:14][OH:15].[OH-].[Na+]>CO>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]=[CH:9][C:10](=[N:14][OH:15])[CH3:11]参加物
5
実験手順
In a 250 ml single neck flask was charged 5.4 g (29.9 mmoles, 1.0 eq.) of (E)-4-(2-chlorophenyl)-3-buten-2-one and 5.2 g (75.4 mmoles, 2.5 eq) of hydroxylamine hydrochloride and 6 g of 50% sodium hydroxide (75 mmoles, 2.5 eq) and 100 ml of methanol. The reaction mixture was stirred at reflux for 2 hours. The reaction mixture was concentrated, diluted with water (50 ml), and then extracted with ethyl acetate (2×50 ml). The organic phase was dried and concentrated, to obtain 3.4 g of 4-(2-chlorophenyl)-3-buten-2-one 2-oxime (E/Z mixture of oximes) as an oil in 58.1% yield.
後処理
- temperatureat reflux for 2 hours
- concentrationThe reaction mixture was concentrated
- additiondiluted with water (50 ml)
- extractionextracted with ethyl acetate (2×50 ml)
- customThe organic phase was dried
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-35a581b6cbf04810b891f5c7c4c14275
- 出典データセット
- uspto-grants-2001_01
- 特許番号
- US06177462B1
反応ノート
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