化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2221755作成日:2026年10月25日
Sodium sulfate decahydrate → {1-benzyl-3-[(6-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-pyridinyl)methoxy]-1H-pyrazol-4-yl}methanol
https://huagongshe.com/reaction/2221755
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium sulfate decahydrate | HCID 62649 | — |
| 反応物 | Aluminium lithium hydride | HCID 21226445 | — |
| 反応物 | ethyl 1-benzyl-3-[(6-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-pyridinyl)methoxy]-1H-pyrazole-4-carboxylate | HCID 69218263 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | {1-benzyl-3-[(6-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-pyridinyl)methoxy]-1H-pyrazol-4-yl}methanol | HCID 69217047 | 95% |
反応手順
To a solution of ethyl 1-benzyl-3-[(6-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-pyridinyl)methoxy]-1H-pyrazole-4-carboxylate (1.00 g) in tetrahydrofuran (30 mL) was added lithium aluminum hydride (0.15 g) at 0° C. and the mixture was stirred at room temperature for 2 hrs. Sodium sulfate decahydrate (1.25 g) was added to the reaction mixture, and the mixture was stirred at room temperature for 30 min. The reaction mixture was diluted with ethyl acetate and the precipitate was filtered off. The filtrate was concentrated to give {1-benzyl-3-[(6-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-pyridinyl)methoxy]-1H-pyrazol-4-yl}methanol as colorless crystals (0.87 g, yield 95%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 94-95° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07368578B2 |
|---|
| 出典データセット | uspto-grants-2008_05 |
|---|
| ORD ID | ord-5e9ee49d35664b19b6de9f83dae63b6d |
|---|
| 出典メモ | uspto-grants-2008_05 |
|---|