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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1092047생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1092047

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Methyl 4-bromobenzoateHCID 12081—
반응물1-IsopropylpiperazineHCID 78013—
촉매2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,2-DimethoxyethaneHCID 8071—
생성물Methyl 4-(4-propan-2-yl-piperazin-1-yl)benzoateHCID 6912977864.8%

반응 조건

온도130 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08129391B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-f048eb6a13a84914a2cb66b95d938966
출처 메모uspto-grants-2012_03