HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890836Generated: October 26, 2026
2-Bromonaphthalene → 2-Bromo-9,10-di-naphthalene-2-yl-9,10-dihydro-anthracene-9,10-diol
https://huagongshe.com/reaction/890836
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromonaphthalene | HCID 11372 | — |
| Reactant | 2-Bromoanthraquinone | HCID 221013 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-9,10-di-naphthalene-2-yl-9,10-dihydro-anthracene-9,10-diol | HCID 22247166 | 93% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06998487B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-03bcbf3dd5ef4e5199d1c034360cbe7f |
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| Source note | uspto-grants-2006_02 |
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