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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25859생성일: 2026년 10월 24일

1-Benzyl-3-bromobenzene → 4-(3'-Benzylphenyl)-3-(S)-iso-propyl-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/25859

반응식

참여 물질

역할이름HCID투입량
반응물1-Benzyl-3-bromobenzeneHCID 597532—
반응물Dichloromethane methanolHCID 21226129—
반응물Sodium t-butoxideHCID 23676156—
반응물(S)-1-Boc-3-isopropylpiperazineHCID 24820348—
촉매2'-(diphenylphosphanyl)-N,N-dimethyl-[1,1'-biphenyl]-2-amineHCID 2734939—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
생성물4-(3'-Benzylphenyl)-3-(S)-iso-propyl-piperazine-1-carboxylic acid tert-butyl esterHCID 6912986959,322%

반응 조건

온도80 °C

반응 단계

9.4 mg (10.3 μmol, 0.013 eq.) Pd2(dba)3 and 11.4 mg (29.9 μmol, 0.04 eq.) 2-Diphenylphosphino-2′-dimethylamino-biphenyl were dissolved in 6 ml dry toluene. Then 170.7 mg (1.78 mmol, 2.32 eq.) NaOt-Bu was added, followed by a solution of 175.0 mg (0.77 mmol) 3-(S)-Isopropyl-piperazine-1-carboxylic acid tert-butyl ester (85) and 290.6 mg (1.18 μmol, 1.54 eq.) 1-Benzyl-3-bromo-benzene (87). The resulting mixture was heated at 80° C. for 22 h. After cooling to room temperature the mixture was diluted with ether and washed with brine. The comb. org. fractions were dried over Na2SO4 and evaporated. Column chromatography (hexanes/EtOAc (3+1)) yielded 276.5 mg (0.70 mmol, 91.49%) 4-(3′-Benzylphenyl)-3-(S)-iso-propyl-piperazine-1-carboxylic acid tert-butyl ester (88).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858600B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-f3e25a85adf64b2aa5d09bac8840401a
출처 메모uspto-grants-2005_02