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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (Z)-Prop-1-en-1-ylboronic acid | HCID 5355539 | — |
| 反応物 | cis-2-benzyl-6-bromo-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole | HCID 70664398 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 溶媒 | Sodium Carbonate | HCID 10340 | — |
| 生成物 | cis-2-benzyl-3a-methyl-6-((Z)-prop-1-enyl)-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole | HCID 70664492 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08729274B2 |
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| 出典データセット | uspto-grants-2014_05 |
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| ORD ID | ord-8669a7ffe1e4458d8a10cb1235145559 |
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| 出典メモ | uspto-grants-2014_05 |
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