反応式
[CH:1]([C:3]1[O:4][C:5]([C:8]([OH:10])=[O:9])=[CH:6][CH:7]=1)=O.Cl.[NH2:12]O.C(OC(=O)C)(=O)C.Cl>O.N1C=CC=CC=1>[C:1]([C:3]1[O:4][C:5]([C:8]([OH:10])=[O:9])=[CH:6][CH:7]=1)#[N:12]参加物
反応条件
- 温度
- 85 °C
実験手順
To 2.8 g of 2-formyl-5-furancarboxylic acid (20 mmol) and 2.7 g of hydroxylamine hydrochloride (40 mmol) under Ar was added and dry pyridine (50 mL). The mixture was heated to 85° C., acetic anhydride (40 mL) was added and the mixture was stirred for 3 h. After cooling to 60° C., water (250 mL) was added and the mixture was stirred at RT for 70 h. The mixture was acidified to pH 2 with concentrated hydrochloric acid and extracted with 3:1 dichloromethane-isopropanol (8×100 mL). The combined organic layers were washed with water (100 mL), brine (100 mL), dried over anh sodium sulfate and concentrated in vacuo to afford the title compound as a tan solid (1.26 g, 46%). 1H-NMR (CD3OD; 400 MHz): δ 14.05 (br s, 1H), 7.74 (d, 1H, J=3.8 Hz), 7.42 (d, 1H, J=3.8 Hz).
後処理
- temperatureAfter cooling to 60° C.
- stirringthe mixture was stirred at RT for 70 h
- extractionextracted with 3:1 dichloromethane-isopropanol (8×100 mL)
- washThe combined organic layers were washed with water (100 mL), brine (100 mL)
- dry with materialdried over anh sodium sulfate
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-c748a3d7b1ef49f59b4233571c04724a
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07427683B2
関連ノート
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