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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274124Generated: October 30, 2026

Methanesulfonic Acid → 5-Bromobenzo[c]phenanthrene

https://huagongshe.com/reaction/2274124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-[2-(2-methoxyvinyl)phenyl]naphthaleneHCID 67607495—
SolventDichloromethaneHCID 6344—
Product5-Bromobenzo[c]phenanthreneHCID 1066248215%

Reaction Steps

180 g of 1-bromo-4-[2-(2-methoxyvinyl)phenyl]naphthalene and 1.0 L of dichloromethane were placed. 25 mL of methanesulfonic acid was added at room temperature while stirring. The stirring was conducted for 8 hours at room temperature. After the completion of the reaction, 1 L of an aqueous solution of 10% potassium carbonate was added. After removing an aqueous phase, an organic phase was washed with water and saturated saline, and dried with magnesium sulfate. After filtering off magnesium sulfate, the organic phase was concentrated. The residues were purified by silica gel column chromatography, whereby 24.4 g (yield 15%) of 5-bromobenzo[c]phenanthrene as an intended product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126943B2
Source datasetuspto-grants-2015_09
ORD IDord-408cf63e92c54a2284cfc0b9890a1ff1
Source noteuspto-grants-2015_09