Hydroxyamine hydrochloride → 5-(Thiophen-2-YL)-1,2-oxazole
反応式
CN(C)[C:3](=[CH2:11])[C:4]([C:6]1[S:7][CH:8]=[CH:9][CH:10]=1)=[O:5].Cl.[NH2:14]O>CO>[S:7]1[CH:8]=[CH:9][CH:10]=[C:6]1[C:4]1[O:5][N:14]=[CH:11][CH:3]=1参加物
4
実験手順
A mixture of Compound 3 (18.1g, 100 mmol) and hydroxylamine hydrochloride (7.0 g, 101 mmol) in 100 mL of anhydrous methanol was refluxed under nitrogen for 2 hours. The reaction mixture was cooled, concentrated and partitioned between water and dichloromethane. The dichloromethane layer was dried with anhydrous sodium sulfate, filtered and concentrated to yield compound 4 as a dark yellow-orange oil (14.1 g, 93.3 mmol, 93%). GC/MS, m/z=151 at tR=8.30 min (100%). LC/MS, [M+H]=152.
後処理
- temperaturewas refluxed under nitrogen for 2 hours
- temperatureThe reaction mixture was cooled
- concentrationconcentrated
- custompartitioned between water and dichloromethane
- dry with materialThe dichloromethane layer was dried with anhydrous sodium sulfate
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-61c270230fe54335aecd3df8e825941c
- 出典データセット
- uspto-grants-2002_05
- 特許番号
- US06384221B1
反応ノート
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