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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217713Generated: October 28, 2026

Citric Acid → 2-Bromo-1-[3-methoxy-5-(1-methylethyl)phenyl]ethanone

https://huagongshe.com/reaction/217713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantWaterHCID 962—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
ReactantHCID 58136851HCID 58136851—
SolventEthyl AcetateHCID 8857—
SolventMeOH tetrahydrofuranHCID 21899815—
Product2-Bromo-1-[3-methoxy-5-(1-methylethyl)phenyl]ethanoneHCID 58136813149.6%

Reaction Steps

1-(3-Isopropyl-5-methoxyphenyl)ethanone (O2.030; 425 mg) was dissolved in methanol/THF 15 ml/15 ml) and admixed while stirring with phenyltrimethylammonium tribromide (831 mg). After stirring at RT for 3 h, the reaction mixture was added to 50 ml of 20% citric acid and stirred for 1 h. After adding water and EA, the EA phase was removed, dried and concentrated. The residue was dissolved in acetonitrile (50 ml), and 2 N sulfuric acid (15 ml) was added to the solution. After standing at RT for 2 h, the mixture was admixed with water and extracted with EA. The EA phase was washed with saturated sodium hydrogencarbonate solution, dried and concentrated. The residue was purified using silica gel (40 g cartridge, n-heptane/EA gradient of 0-50% within 30 min). 520 mg of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198272B2
Source datasetuspto-grants-2012_06
ORD IDord-ee5827def27d49579bce2f0874f56464
Source noteuspto-grants-2012_06