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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117997Generated: October 30, 2026

Water → 3-Bromo-6-(cyclopropylmethoxy)phenanthrene

https://huagongshe.com/reaction/2117997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantBromomethylcyclopropaneHCID 81503—
ReactantHCID 86614876HCID 86614876—
CatalystPotassium IodideHCID 4875—
SolventAcetoneHCID 180—
Product3-Bromo-6-(cyclopropylmethoxy)phenanthreneHCID 8661487887%

Reaction Steps

A mixture of 6-bromophenanthren-3-ol (0.823 g, 3.02 mmol) from Step 1 above, (bromomethyl)cyclopropane (0.5 mL, 5.4 mmol), potassium carbonate (2.5 g, 18 mmol) and potassium iodide (5 mg) in acetone (50 mL) was heated at reflux for 3 days. Water was then added and the reaction mixture extracted with ethyl acetate The organic layer washed with brine, dried over MgSO4, filtered and concentrated. The crude material was purified by flash chromatography on silica (100% hexanes) to provide 3-bromo-6-(cyclopropylmethoxy)phenanthrene (0.859 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442716B2
Source datasetuspto-grants-2008_10
ORD IDord-b105fbd6f0ee4133b18ce07ef66abaa5
Source noteuspto-grants-2008_10