戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1026629作成日:2026年10月27日

(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

反応式

関与物質

役割名称HCID仕込み量
反応物(Z)-Prop-1-en-1-ylboronic acidHCID 5355539—
反応物cis-2-benzyl-6-bromo-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindoleHCID 70664398—
溶媒EthanolHCID 702—
溶媒1,2-DimethoxyethaneHCID 8071—
溶媒Sodium CarbonateHCID 10340—
生成物cis-2-benzyl-3a-methyl-6-((Z)-prop-1-enyl)-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindoleHCID 70664492—

反応条件

温度160 °C

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08729274B2
出典データセットuspto-grants-2014_05
ORD IDord-8669a7ffe1e4458d8a10cb1235145559
出典メモuspto-grants-2014_05