戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1069120作成日:2026年10月24日

4-Thiazolidinone, 3-methyl-2-thioxo- → 5-[[4-[(4-Acetyl-3-hydroxy-2-propylphenyl)methoxy]phenyl]methylene]-3-methyl-2-thioxo-4-thiazolidinone

https://huagongshe.com/ja/reaction/1069120

反応式

関与物質

役割名称HCID仕込み量
反応物4-Thiazolidinone, 3-methyl-2-thioxo-HCID 72900—
反応物Sodium AcetateHCID 517045—
反応物4-[(4-Acetyl-3-hydroxy-2-propylphenyl)methoxy]benzaldehydeHCID 21191277—
溶媒Acetic AcidHCID 176—
生成物5-[[4-[(4-Acetyl-3-hydroxy-2-propylphenyl)methoxy]phenyl]methylene]-3-methyl-2-thioxo-4-thiazolidinoneHCID 86752507—

反応条件

温度100 °C

反応手順

Under a nitrogen atmosphere in a three-neck round bottom flask 4-[(4-acetyl-3-hydroxy-2-propylphenyl)methoxy]benzaldehyde (90.0 mg, 0.29 mmol) was dissolved in acetic acid (1.5 ml) with stirring. To this solution was added sodium acetate (82.8 mg, 1.00 mmol) and N-methylrhodanine (42.5 mg, 0.29 mmol). The reaction mixture was then heated to 100° C. and maintained at this temperature for about two hours at which time the reaction mixture was raised to the reflux temperature and allowed to reflux for about 28 hours. The reaction progress was monitored by thin layer chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06251928B1
出典データセットuspto-grants-2001_06
ORD IDord-03a655ea75a4460ca91808761dd55d17
出典メモuspto-grants-2001_06