Chinese Journal of Organic Chemistry ›› 2026, Vol. 46 ›› Issue (2): 496-506.DOI: 10.6023/cjoc202507037 Previous Articles Next Articles
ARTICLES
收稿日期:2025-07-28
修回日期:2025-09-25
发布日期:2025-11-05
通讯作者:
陈雪冰
基金资助:
Wanting Liang, Siyi Chen, Enqi Xu, Xuebing Chen*(
)
Received:2025-07-28
Revised:2025-09-25
Published:2025-11-05
Contact:
Xuebing Chen
Supported by:Share
Wanting Liang, Siyi Chen, Enqi Xu, Xuebing Chen. Copper-Catalyzed Cyclization Reaction of 3-Nitrochromenes with Enaminones to Synthesize of 2H-Chromeno-pyrrole Derivatives[J]. Chinese Journal of Organic Chemistry, 2026, 46(2): 496-506.
| Entry | Solvent | Promoter | Metal | T/℃ | Yieldb/% |
|---|---|---|---|---|---|
| 1 | EtOH | — | — | r.t.~reflux | N.R. |
| 2 | EtOH | DBU | CuCl2 | r.t. | 25 |
| 3 | EtOH | DBU | CuBr | r.t. | 30 |
| 4 | EtOH | DBU | CuI | r.t. | 30 |
| 5 | EtOH | DBU | AgNO3 | r.t. | 28 |
| 6 | EtOH | DBU | Fe2O3 | r.t. | 10 |
| 7 | EtOH | DBU | FeCl3 | r.t. | 7 |
| 8 | EtOH | DBU | InCl3 | r.t. | 26 |
| 9 | CH3OH | DBU | CuI | r.t. | 25 |
| 10 | Toluene | DBU | CuI | r.t. | 45 |
| 11 | DMSO | DBU | CuI | r.t. | 40 |
| 12 | CH3CN | DBU | CuI | r.t. | 45 |
| 13 | DMF | DBU | CuI | r.t. | 15 |
| 14 | 1,4-Dioxane | DBU | CuI | r.t. | N.R. |
| 15 | THF | DBU | CuI | r.t. | 40 |
| 16 | CH3CN | DBN | CuI | r.t | 51 |
| 17 | CH3CN | Cs2CO3 | CuI | r.t | 38 |
| 18 | CH3CN | K2CO3 | CuI | r.t | 35 |
| 19 | CH3CN | Piperidine | CuI | r.t | 10 |
| 20 | CH3CN | TEA | CuI | r.t | 20 |
| 21 | CH3CN | DABCO | CuI | r.t | 10 |
| 22 | CH3CN | CF3COOH | CuI | r.t | N.R. |
| 23 | CH3CN | TsOH | CuI | r.t | N.R. |
| 24c | CH3CN | DBN | CuI | r.t. | 44 |
| 25d | CH3CN | DBN | CuI | r.t. | 50 |
| 26 | CH3CN | DBN | CuI | 60 | 45 |
| 27 | CH3CN | — | CuI | r.t | N.R. |
| 28 | CH3CN | DBN | — | r.t | 5 |
| Entry | Solvent | Promoter | Metal | T/℃ | Yieldb/% |
|---|---|---|---|---|---|
| 1 | EtOH | — | — | r.t.~reflux | N.R. |
| 2 | EtOH | DBU | CuCl2 | r.t. | 25 |
| 3 | EtOH | DBU | CuBr | r.t. | 30 |
| 4 | EtOH | DBU | CuI | r.t. | 30 |
| 5 | EtOH | DBU | AgNO3 | r.t. | 28 |
| 6 | EtOH | DBU | Fe2O3 | r.t. | 10 |
| 7 | EtOH | DBU | FeCl3 | r.t. | 7 |
| 8 | EtOH | DBU | InCl3 | r.t. | 26 |
| 9 | CH3OH | DBU | CuI | r.t. | 25 |
| 10 | Toluene | DBU | CuI | r.t. | 45 |
| 11 | DMSO | DBU | CuI | r.t. | 40 |
| 12 | CH3CN | DBU | CuI | r.t. | 45 |
| 13 | DMF | DBU | CuI | r.t. | 15 |
| 14 | 1,4-Dioxane | DBU | CuI | r.t. | N.R. |
| 15 | THF | DBU | CuI | r.t. | 40 |
| 16 | CH3CN | DBN | CuI | r.t | 51 |
| 17 | CH3CN | Cs2CO3 | CuI | r.t | 38 |
| 18 | CH3CN | K2CO3 | CuI | r.t | 35 |
| 19 | CH3CN | Piperidine | CuI | r.t | 10 |
| 20 | CH3CN | TEA | CuI | r.t | 20 |
| 21 | CH3CN | DABCO | CuI | r.t | 10 |
| 22 | CH3CN | CF3COOH | CuI | r.t | N.R. |
| 23 | CH3CN | TsOH | CuI | r.t | N.R. |
| 24c | CH3CN | DBN | CuI | r.t. | 44 |
| 25d | CH3CN | DBN | CuI | r.t. | 50 |
| 26 | CH3CN | DBN | CuI | 60 | 45 |
| 27 | CH3CN | — | CuI | r.t | N.R. |
| 28 | CH3CN | DBN | — | r.t | 5 |
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