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Pyridine → Methyl 4-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Methyl 4-(chlorocarbonyl)benzoate | HCID 81850 | — |
| 反応物 | HCID 178419015 | HCID 178419015 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Methyl 4-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzoate | HCID 22934530 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07223791B2 |
| 出典データセット | uspto-grants-2007_05 |
| ORD ID | ord-85b4e8b78b974d90a7e9276c1c60f5d2 |
| 出典メモ | uspto-grants-2007_05 |