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HRID 44784作成日:2026年10月23日
2,2-Dimethyl-1,3-dioxane-4,6-dione → 5-{[(5-Bromopyridin-3-yl)imino]methyl}-2,2-dimethyl-1,3-dioxane-4,6-dione
https://huagongshe.com/ja/reaction/44784
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
| 反応物 | Ethyl orthoformate | HCID 31214 | — |
| 反応物 | 3-Amino-5-bromopyridine | HCID 817681 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-{[(5-Bromopyridin-3-yl)imino]methyl}-2,2-dimethyl-1,3-dioxane-4,6-dione | HCID 57515569 | 300.8% |
反応手順
A mixture of triethyl orthoformate (10 mL, 60.1 mmol) and 2,2-dimethyl-[1,3]-dioxane-4,6-dione (40.9 g, 0.23 mol) (Meldrum's acid) was heated at 92° C. for 90 minutes and then cooled to 70° C. over one hour. 3-Amino-5-bromopyridine (40.9 g, 0.20 mol) was slowly added over 10 minutes with an ethanol rinse while maintaining the reaction temperature between 60 and 70° C. The reaction was then heated for an additional 20 minutes and allowed to cool to room temperature. The reaction mixture was filtered and washed with ethanol (150 mL) yielding a tan solid. The solid was dried under vacuum for 2 hours to yield 59.14 g of 5-{[(5-bromopyridin-3-yl)imino]methyl}-2,2-dimethyl-1,3-dioxane-4,6-dione as a light yellow crystalline solid, mp 200-202° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08541438B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-09c09cade9a24ce5aa5d5eebe631ea7b |
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| 出典メモ | uspto-grants-2013_09 |
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