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HRID 2221786作成日:2026年10月27日
Sodium sulfate decahydrate → {3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-phenyl-1H-pyrazol-4-yl}methanol
https://huagongshe.com/reaction/2221786
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sodium sulfate decahydrate | HCID 62649 | — |
| 反応物 | Aluminium lithium hydride | HCID 21226445 | — |
| 反応物 | ethyl 3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-phenyl-1H-pyrazole-4-carboxylate | HCID 69216028 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | {3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-phenyl-1H-pyrazol-4-yl}methanol | HCID 69218022 | 98% |
反応手順
To a solution of ethyl 3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-phenyl-1H-pyrazole-4-carboxylate (2.44 g) in tetrahydrofuran (50 mL) was added lithium aluminum hydride (0.17 g) at 0° C. and the mixture was stirred at room temperature for 1 hr. Sodium sulfate decahydrate (1.48 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 {3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-phenyl-1H-pyrazol-4-yl}methanol as colorless crystals (2.20 g, yield 98%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 127-128° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07368578B2 |
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| 出典データセット | uspto-grants-2008_05 |
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| ORD ID | ord-b248af9c4be5415aae606a0f7391a39c |
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| 出典メモ | uspto-grants-2008_05 |
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