HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1610784Erstellt: 25. Oktober 2026
2-Bromonaphthalene → 2-Bromo-9,10-di-naphthalene-2-yl-9,10-dihydro-anthracene-9,10-diol
https://huagongshe.com/reaction/1610784
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Bromonaphthalene | HCID 11372 | — |
| Edukt | 2-Bromoanthraquinone | HCID 221013 | — |
| Edukt | HCID 178418306 | HCID 178418306 | — |
| Lösungsmittel | Pentane | HCID 8003 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Bromo-9,10-di-naphthalene-2-yl-9,10-dihydro-anthracene-9,10-diol | HCID 22247166 | 93% |
Reaktionsschritte
To a solution of 2-bromonaphthalene (6.49 g, 31.3 mmol) in dry THF (50 ml) was added dropwise t-BuLi (18.4 ml of a 1.7 M solution in pentane) at −78° C. under nitrogen. After the mixture had been stirred for 30 min, 2-bromoanthraquinone (3.00 g, 10.4 mmol) was added at −78° C. The cooling bath was removed and the mixture was stirred for 2 hours at room temperature. The mixture was quenched with saturated aqueous ammonium chloride solution (50 ml) and extracted with ethyl ether (3×50 ml). The combined organic extracts were dried over MgSO4 and concentrated under vacuum. The crude product was slurried in petroleum ether, filtered off with suction, and washed with petroleum ether. After drying, the 2-bromo-9,10-di-naphthalene-2-yl-9,10-dihydro-anthracene-9,10-diol (5.30 g, 93%) was obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06984462B2 |
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| Quelldatensatz | uspto-grants-2006_01 |
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| ORD ID | ord-e36c353889f04976be3e3322e335d23f |
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| Quellennotiz | uspto-grants-2006_01 |
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