戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 352083作成日:2026年10月26日

p-Toluenesulfonic acid monohydrate → 1-[4-[4-[[2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazol-4-yl]methoxy]phenyl]butyl]-1H-1,2,3-triazole p-toluenesulfonate

https://huagongshe.com/reaction/352083

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物MubritinibHCID 6444692—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物1-[4-[4-[[2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazol-4-yl]methoxy]phenyl]butyl]-1H-1,2,3-triazole p-toluenesulfonateHCID 2271504180.4%

反応手順

1-[4-[4-[[2-[(E)-2-[4-(Trifluoromethyl)phenyl]ethenyl]-1,3-oxazol-4-yl]methoxy]phenyl]butyl]-1H-1,2,3-triazole (1.0 g) was dissolved in ethyl acetate (50 ml) and tetrahydrofuran (5 ml). A solution of p-toluenesulfonic acid monohydrate (406 mg) in tetrahydrofuran (5 ml) was added dropwise. The crystals were precipitated. The mixture was stirred at room temperature for 2 hours 20 min and filtrated. The mixture was washed with ethyl acetate/isopropyl ether=1/1 (3 ml) and dried under reduced pressure (40° C.) to give 1-[4-[4-[[2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazol-4-yl]methoxy]phenyl]butyl]-1H-1,2,3-triazole p-toluenesulfonate (1.1 g, yield 80%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06743924B2
出典データセットuspto-grants-2004_06
ORD IDord-83ea170c387d4a01b2e04dca1a9bf9a6
出典メモuspto-grants-2004_06