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HRID 16777作成日:2026年10月23日

Potassium Carbonate → Methyl 4-(4-propan-2-yl-piperazin-1-yl)benzoate

https://huagongshe.com/ja/reaction/16777

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Methyl 4-bromobenzoateHCID 12081—
反応物1-IsopropylpiperazineHCID 78013—
触媒2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物Methyl 4-(4-propan-2-yl-piperazin-1-yl)benzoateHCID 6912977864.8%

反応条件

温度130 °C

反応手順

Tris(dibenzylideneacetone)dipalladium(0) (0.014 g, 0.02 mmol) was added to a deoxygenated suspension of 1-isopropylpiperazine (0.151 g, 1.18 mmol), methyl 4-bromobenzoate (0.215 g, 1 mmol), potassium carbonate (0.193 g, 1.4 mmol) and 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (0.012 g, 0.03 mmol) in DME (4 mL), and sealed into a microwave tube. The reaction was heated to 130° C. for 10 mins in the microwave reactor and cooled to room temperature. The reaction mixture was evaporated to dryness, redissolved in EtOAc (25 mL) and washed sequentially with water (15 mL) and saturated brine (15 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by silica column chromatography, eluting with 5% MeOH in DCM. Pure fractions were evaporated to dryness to afford methyl 4-(4-propan-2-yl-piperizin-1-yl)benzoate (0.170 g, 64.8%) as a tan solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737149B2
出典データセットuspto-grants-2010_06
ORD IDord-4f87b8ae39c644da980c51f4ff0bae70
出典メモuspto-grants-2010_06