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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405459Generated: October 31, 2026

Methanesulfonic Acid → 5-Bromobenzo[c]phenanthrene

https://huagongshe.com/reaction/2405459

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

A reaction vessel was charged with 180 g of 1-bromo-4-[2-(2-methoxyvinyl)phenyl]naphthalene and 1.0 L of dichloromethane. 25 mL of methanesulfonic acid was added to the mixture at room temperature with stirring. The mixture was stirred at room temperature for 8 hours. After completion of the reaction, 1 L of a 10% potassium carbonate aqueous solution was added to the mixture. After removing the aqueous phase, the organic phase was washed with water and a saturated sodium chloride solution, and dried over magnesium sulfate. After removing magnesium sulfate by filtration, the organic phase was concentrated. The residue was purified by silica gel column chromatography to obtain 24.4 g of the target 5-bromobenzo[c]phenanthrene (yield: 15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08803420B2
Source datasetuspto-grants-2014_08
ORD IDord-ff606c0e99c74b8a8c46bb0b36d49424
Source noteuspto-grants-2014_08