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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670163Generated: October 30, 2026

Dimethyl Sulfoxide → 2,6-dibromo-8,9-dihydro-4H-cyclopenta[def]phenanthrene

https://huagongshe.com/reaction/1670163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantHexamethylphosphoramideHCID 12679—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2,6-dibromo-4H-cyclopenta[def]phenanthreneHCID 59431076—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2,6-dibromo-8,9-dihydro-4H-cyclopenta[def]phenanthreneHCID 12524367133.6%

Reaction Steps

2,6-dibromo-4H-cyclopenta[def]phenanthrene (2.6 g, 7.7 mmol), t-BuOK (20.8 g, 61.6 mmol), DMSO (20 ml), and HMPA (20 ml) was placed in 50 ml round bottom flask with a syringe. The mixture was stirred for 50 minutes at room temperature and cooled to 0° C. CH3l (3.75 ml, 61.6 mmol) was dropped to the mixture with a syringe and the resultant solution was stirred for 30 minutes at 0° C. Then, water (50 ml) and methylene chloride (50 ml) were added to the solution to separate an organic layer. The organic layer was purified by silica gel column chromatography to obtain compound 2 (3.6 g, 80%). 1H NMR (300 MHz, CDCl3, δ): 7.98(2H, s), 7.79(2H, s), 7.73(2H, s), 1.93(m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07990053B2
Source datasetuspto-grants-2011_08
ORD IDord-2cdff173bf2b4a92890a3ab49060b296
Source noteuspto-grants-2011_08