関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzaldehyde | HCID 240 | — |
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Cinnamoylbenzene | HCID 7189 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | 2,2,4-Triphenyl-butane-1,4-dione | HCID 21425062 | — |
反応手順
Following the procedure described in Example 1, 57.2 g (0.275 mol) of benzylideneacetophenone, 29.2 g of benzaldehyde, 25.1 g (0.1 mol) of Catalyst 2 and 400 ml of dimethylformamide are introduced successively into the 500 ml three-necked flask and after stirring for 15 minutes under nitrogen 40.4 g (0.4 mol) of triethylamine are added. The mixture is then heated to 80° C for 12 hours. For working up, the dimethylformamide is distilled off and 150 ml of isopropanol are added to the residue while it is still hot. The product which has precipitated is filtered off, washed with isopropanol and then dried. 2,2,4-Triphenyl-butane-1,4-dione is obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04035395 |
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| 出典データセット | uspto-grants-1977_07 |
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| ORD ID | ord-091d27a4e217419a895418ea1b77f057 |
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| 出典メモ | uspto-grants-1977_07 |
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