Ethyl 3-hydroxyfuro[2,3-c]pyridine-2-carboxylate → Furo[2,3-C]pyridin-3(2H)-one
反応式
C(OC([C:6]1[O:14][C:9]2=[CH:10][N:11]=[CH:12][CH:13]=[C:8]2[C:7]=1[OH:15])=O)C>Cl.O>[O:14]1[C:9]2=[CH:10][N:11]=[CH:12][CH:13]=[C:8]2[C:7](=[O:15])[CH2:6]1参加物
4
実験手順
A suspension of 3-hydroxyfuro[2,3-c]pyridine-2-carboxylic acid ethyl ester (10 mmol) in 10 mL 25% HCl solution and 5 mL H2O was heated to reflux overnight. After cooling to RT, the reaction mixture was quenched with sat. aq. NaHCO3 solution and extracted with EtOAc. The combined organic layers were dried over MgSO4 and concentrated in vacuo to give the desired product as brown solid;
後処理
- temperaturewas heated
- temperatureto reflux overnight
- customthe reaction mixture was quenched with sat. aq. NaHCO3 solution
- extractionextracted with EtOAc
- dry with materialThe combined organic layers were dried over MgSO4
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-e8465752acde40e68505e484cd7c1730
- 出典データセット
- uspto-grants-2015_12
- 特許番号
- US09221832B2
反応ノート
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