HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 62234Erstellt: 24. Oktober 2026
Morpholine → 6-Methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one
https://huagongshe.com/de/reaction/62234
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Morpholine | HCID 8083 | — |
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | Binap, (A+-)- | HCID 634876 | — |
| Edukt | 5-Bromo-6-methoxy-1-indanone | HCID 22278718 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 6-Methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one | HCID 117940128 | — |
Reaktionsschritte
A solution of 5-bromo-6-methoxy-2,3-dihydro-1H-inden-1-one (11) (1 g, 4.149 mmol) and morpholine (0.36 g, 4.149 mmol) in toluene 15 mL was added cesium carbonate (2.69 g, 8.298 mmol). The reaction was degassed and purged with nitrogen for 10 min. Pd2(dba)3 (189.3 mg, 0.207 mmol) and BINAP (64.5 mg, 0.103 mmol) was added, degassed and purged and with nitrogen for another 10 min. The reaction was heated to 110° C. overnight under sealed microwave vial. After completion of the starting material, the reaction was diluted with chloroform and filtered through celite bed. The organic layer was concentrated to get the crude compound 13 and the resulting crude was purified through flash chromatography by using 100-200 mesh silica gel eluting the compound at 25% ethyl acetate in hexane as pale yellow coloured solid 6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one 13. 1HNMR (400 MHz, CDCl3) δ ppm 7.70 (s, 1H), 7.20 (s, 1H), 3.93 (s, 3H), 3.06 (m, 2H), 2.72 (m, 2H); MS (ESI) m/z 247.9 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09446047B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-91e0d8a9e1ae4f0c8f4fbc35dca47205 |
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| Quellennotiz | uspto-grants-2016_09 |
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