参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 对溴苯甲酸甲酯 | HCID 12081 | — |
| 反应物 | POTASSIUM DIPHOSPHATE | HCID 62657 | — |
| 反应物 | 1-乙酰哌嗪 | HCID 83795 | — |
| 反应物 | 2-双环己基膦-2',6'-二甲氧基联苯 | HCID 11269872 | — |
| 溶剂 | 甲苯 | HCID 1140 | — |
| 产物 | Methyl 4-(4-acetylpiperazin-1-yl)benzoate | HCID 57440409 | 56.2% |
反应步骤
A deoxygenated suspension of 1-acetylpiperazine (0.308 g, 2.40 mmol), methyl 4-bromobenzoate (0.430 g, 2 mmol), tri-potassium orthophosphate (0.594 g, 2.80 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (0.164 g, 0.40 mmol) and tris(dibenzylideneacetone)dipaladium(0) (0.092 g, 0.10 mmol) in toluene (10 mL) was stirred at 100° C., over a period of 24 h under nitrogen. The cooled reaction mixture was filtered and evaporated to give crude product. The crude product was purified by silica column chromatography, eluting with a gradient 0-5% MeOH in DCM. Pure fractions were evaporated to dryness to afford methyl 4-(4-acetylpiperazin-1-yl)benzoate (0.295 g, 56.2%) as a yellow solid.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US07737149B2 |
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| 来源数据集 | uspto-grants-2010_06 |
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| ORD ID | ord-743a010bd61e44b484bd996ac6892806 |
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| 来源说明 | uspto-grants-2010_06 |
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