反応式
[NH2:1][C:2]1[CH:7]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[CH:5]=[CH:4][C:3]=1[OH:12].[K+].C(O[C:17]([S-])=[S:18])C.Cl>N1C=CC=CC=1>[CH3:11][O:10][C:8]([C:6]1[CH:5]=[CH:4][C:3]2[O:12][C:17](=[S:18])[NH:1][C:2]=2[CH:7]=1)=[O:9]参加物
5
実験手順
In a round bottom flask equipped with a mechanical stirrer, reflux condenser and drying tube were placed 2-amino-4-methoxycarbonylphenol (8,3 g, 0.05 mole), O-ethylxanthic acid potassium salt (8.8 g, 0.055 mole) and pyridine (125 mL). The mixture was stirred and heated at reflux for 2 hours and cooled to room temperature. The mixture was poured into ice and concentrated HCl (50 mL). The product was collected as a solid and washed thoroughly with water. The material was air dried to give 9.9 g (95%) of the 5-methoxycarbonylbenzoxazol-2-thione as a white powder, m.p. 218°-221° C.
後処理
- customIn a round bottom flask equipped with a mechanical stirrer
- temperaturereflux condenser
- customdrying tube
- temperatureheated
- temperatureat reflux for 2 hours
- customThe product was collected as a solid
- washwashed thoroughly with water
- customdried
出典と根拠
- ORDレコード
- ord-8fd265b3a6134e339dc6418af3aae6b0
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05413905
関連ノート
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