HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1509656Erstellt: 25. Oktober 2026
Pivalic acid → 3-Chloro-10,11-dihydro-5H-benzo(d)naphtho(2,3-b)pyran-8(9H)-one
https://huagongshe.com/reaction/1509656
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pivalic acid | HCID 6417 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 7-((2-Bromo-5-chlorophenyl)methoxy)-1,2,3,4-tetrahydronaphthalen-1-one | HCID 69672813 | — |
| Katalysator | Tris(4-fluorophenyl)phosphine | HCID 140387 | — |
| Katalysator | palladium(II) pivalate | HCID 24905427 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 3-Chloro-10,11-dihydro-5H-benzo(d)naphtho(2,3-b)pyran-8(9H)-one | HCID 69673366 | 67% |
Reaktionsschritte
To a 1 L flask containing palladium(II) pivalate (1.18 g, 3.8 mmol), tri(4-fluorophenyl)phosphine (1.20 g, 3.8 mmol), pivalic acid (2.33 g, 22.8 mmol) and potassium carbonate (31.8 g, 228 mmol) was added a solution of 7-(2-bromo-5-chlorobenzyloxy)-3,4-dihydronaphthalen-1(2H)-one (27.8 g, 76.2 mmol) in dimethylacetamide (380 mL). The flask was evacuated and backfilled with argon 5 times and then stirred under argon at 60° C. for 24 hours. The reaction was cooled to room temperature and diluted with MTBE and water. The resulting biphasic mixture was stirred for 3 hours and filtered through Celite, rinsing with MTBE. The organic layer of the filtrate was separated and then washed twice with water and once with brine. The organics were then dried with magnesium sulfate, filtered, concentrated and purified by flash column chromatography (Hexanes/DCM) to yield 3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (14.4 g, 67% yield) as an off-white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09221833B2 |
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| Quelldatensatz | uspto-grants-2015_12 |
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| ORD ID | ord-0cc3e788100b4969ac6ad53794bd3728 |
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| Quellennotiz | uspto-grants-2015_12 |
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