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HRID 16785生成日期:2026年10月23日

对溴苯甲酸甲酯 → Methyl 4-(4-acetylpiperazin-1-yl)benzoate

https://huagongshe.com/zh-CN/reaction/16785

反应方程式

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 DIPHOSPHATEHCID 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)benzoateHCID 5744040956.2%

反应条件

温度100 °C

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

DOI10.6084/m9.figshare.5104873.v1
专利号US07737149B2
来源数据集uspto-grants-2010_06
ORD IDord-743a010bd61e44b484bd996ac6892806
来源说明uspto-grants-2010_06