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HRID 1354453作成日:2026年10月27日

Pyridine → Methyl 4-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzoate

https://huagongshe.com/reaction/1354453

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Methyl 4-(chlorocarbonyl)benzoateHCID 81850—
反応物HCID 178419015HCID 178419015—
溶媒WaterHCID 962—
生成物Methyl 4-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzoateHCID 2293453092%

反応手順

A mixture of methyl 4-chloroformylbenzoate (1.17 g), 5-(4-t-butylphenyl)-1H-tetrazole (1.00 g) and pyridine (10 ml) was heated under reflux for 1 hr. After cooling, water was added to the mixture. The crystals were collected by filtration and dissolved in ethyl acetate. This solution was washed with 1 M hydrochloric acid, water and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was washed with cold hexane to give methyl 4-[5-(4-t-butylphenyl)-1,3,4-oxadiazol-2-yl]benzoate (1.51, yield 92%). Recrystallization from hexane-tetrahydrofuran gave colorless prism crystals. melting point: 210–211° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07223791B2
出典データセットuspto-grants-2007_05
ORD IDord-85b4e8b78b974d90a7e9276c1c60f5d2
出典メモuspto-grants-2007_05