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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1026629생성일: 2026년 10월 25일

(Z)-Prop-1-en-1-ylboronic acid → cis-2-benzyl-3a-methyl-6-((Z)-prop-1-enyl)-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole

https://huagongshe.com/reaction/1026629

반응식

참여 물질

역할이름HCID투입량
반응물(Z)-Prop-1-en-1-ylboronic acidHCID 5355539—
반응물cis-2-benzyl-6-bromo-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindoleHCID 70664398—
용매EthanolHCID 702—
용매1,2-DimethoxyethaneHCID 8071—
용매Sodium CarbonateHCID 10340—
생성물cis-2-benzyl-3a-methyl-6-((Z)-prop-1-enyl)-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindoleHCID 70664492—

반응 조건

온도160 °C

반응 단계

Tetrakis(triphenylphosphine)Pd(0) (0.021 mmol, 24.32 mg) was added in one portion to a mixture of cis-2-benzyl-6-bromo-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole (0.421 mmol, 150 mg) and (Z)-prop-1-enylboronic acid (0.631 mmol, 54.2 mg) in 2 N aq Na2CO3 (1 ml), DME (1 ml) and EtOH (0.5 ml) The reaction mixture was heated under microwave irradiation at 160° C. for 900 seconds and then the mixture was filtered through celite. The resulting filtrate was diluted with water and extracted with DCM (3×). The combined organic extracts were dried over Na2SO4 and conc in vauco to afford a brown oil that was purified by silica column chromatography (eluting with 10% EtOAc in heptane) to afford cis-2-benzyl-3a-methyl-6-((Z)-prop-1-enyl)-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole) (127 mg), m/z: 318.3 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08729274B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-8669a7ffe1e4458d8a10cb1235145559
출처 메모uspto-grants-2014_05