HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 902553Erstellt: 25. Oktober 2026
4-Heptanone → 4-(7-bromo-2-methyl-2H-indazol-3-yl)-heptan-4-ol
https://huagongshe.com/reaction/902553
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Heptanone | HCID 31246 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Edukt | 7-bromo-2-methyl-2H-indazole | HCID 21094580 | — |
| Edukt | Tetrahydrofuran heptane ethylbenzol | HCID 22742125 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-(7-bromo-2-methyl-2H-indazol-3-yl)-heptan-4-ol | HCID 21094589 | 78% |
Reaktionsschritte
To a solution of 7-bromo-2-methyl-2H-indazole (1.5 g, 7.1 mmol) in 18 mL of THF at −78° C. was added a 2 M solution of lithium diisopropylamide in heptane/ethylbenzene/THF (5.3 mL, 11 mmol). The solution was stirred at 0-5° C. for 10 m, then rechilled to −78° C. To it was added 4-heptanone (1.49 mL, 10.6 mmol), and the solution was stirred overnight, allowing to slowly warm to room temperature. A saturated aqueous NaHCO3 solution (40 mL) was added, and the mixture was extracted with three 30 mL portions of ethyl acetate. The combined organic layers were dried over Na2SO4, filtered, and concentrated to a brown solid. Column chromatography (0→20% EtOAc/hexanes) afforded 4-(7-bromo-2-methyl-2H-indazol-3-yl)-heptan-4-ol (42; 1.80 g; 78%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07365211B2 |
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| Quelldatensatz | uspto-grants-2008_04 |
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| ORD ID | ord-ef09b8f2e6f547d09b8fcedd28f5bf1f |
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| Quellennotiz | uspto-grants-2008_04 |
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