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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097533Generated: October 31, 2026

Methanol → 2-Bromo-1-[3-(cyclopentyloxy)-4-methoxyphenyl]ethan-1-one

https://huagongshe.com/reaction/2097533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(3-(Cyclopentyloxy)-4-methoxyphenyl)ethanoneHCID 11746579—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
SolventWaterHCID 962—
Product2-Bromo-1-[3-(cyclopentyloxy)-4-methoxyphenyl]ethan-1-oneHCID 5443850541.7%

Reaction Steps

To 200 ml of methanol solution containing 11.6 g (49.5 mmol) of 1-(3-cyclopentoxy-4-methoxyphenyl)ethanone (see Bioorg. Med. Chem. Lett. 2003, 13, 2355) was added 20.47 g (54.5 mmol) of trimethylphenylammonium tribromide at room temperature, and the mixture was stirred at room temperature for 40 minutes. After completion of the reaction, water was added to the reaction mixture, and the mixture was neutralized with a saturated aqueous solution of sodium hydrogencarbonate and then extracted with chloroform. The organic layer after separation was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. To the obtained concentrate was added 50 ml of a mixed solvent (diisopropyl ether/hexane=1/2 (V/V)), and precipitated solid was collected by filtration. The obtained solid was washed with diisopropyl ether, and dried under reduced pressure to obtain 6.47 g of the title compound as a white solid. (Yield: 41%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450319B2
Source datasetuspto-grants-2013_05
ORD IDord-24ecabb0cb184d8087b4dfdf88b4c9e4
Source noteuspto-grants-2013_05