反応式
O=[C:2]1[CH:6]([C:7]([O:9][CH3:10])=[O:8])[CH2:5][S:4][CH2:3]1.[ClH:11].[NH2:12]O>CO>[ClH:11].[NH2:12][C:2]1[C:6]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][S:4][CH:3]=1参加物
4
実験手順
3-Oxo-4-methoxycarbonyltetrahydrothiophene (28 g) was heated under reflux for 1 hour with hydroxylamine hydrochloride (11.5 g) in methanol (80 ml). The mixture was then cooled and a first crop was filtered off and washed with dry diethyl ether to afford the title compound (18.4 g, 57.6%) m.p. 203° to 205° C. On further cooling a second crop (2.7 g, 8.5%) was obtained, m.p. 201° to 202° C. The total yield was thus 66.1%.
後処理
- temperatureThe mixture was then cooled
- filtrationa first crop was filtered off
- washwashed with dry diethyl ether
出典と根拠
- ORDレコード
- ord-bfaff0b14b7248de9e161e3a59afa063
- 出典データセット
- uspto-grants-1989_07
- 特許番号
- US04847386
関連ノート
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