HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1026629Erstellt: 26. Oktober 2026
(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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | (Z)-Prop-1-en-1-ylboronic acid | HCID 5355539 | — |
| Edukt | cis-2-benzyl-6-bromo-3a-methyl-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole | HCID 70664398 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | 1,2-Dimethoxyethane | HCID 8071 | — |
| Lösungsmittel | Sodium Carbonate | HCID 10340 | — |
| Produkt | cis-2-benzyl-3a-methyl-6-((Z)-prop-1-enyl)-2,3,3a,4,5,9b-hexahydro-1H-benzo[e]isoindole | HCID 70664492 | — |
Reaktionsschritte
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]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08729274B2 |
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| Quelldatensatz | uspto-grants-2014_05 |
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| ORD ID | ord-8669a7ffe1e4458d8a10cb1235145559 |
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| Quellennotiz | uspto-grants-2014_05 |
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