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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217716Generated: October 30, 2026

Citric Acid → 2-Bromo-1-[3-morpholin-4-yl-5-(pentafluorosulfanyl)phenyl]ethanone

https://huagongshe.com/reaction/217716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantDichloromethaneHCID 6344—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
Reactant1-[3-Morpholin-4-yl-5-(pentafluorosulfanyl)phenyl]ethanoneHCID 58136786—
SolventMeOH tetrahydrofuranHCID 21899815—
Product2-Bromo-1-[3-morpholin-4-yl-5-(pentafluorosulfanyl)phenyl]ethanoneHCID 58136912109.5%

Reaction Steps

1-[3-Morpholin-4-yl-5-(pentafluorosulfanyl)phenyl]ethanone (O2.044; 1.1 g) was dissolved in methanol/THF (20/20 ml) and admixed while stirring with phenyltrimethylammonium tribromide (1.25 g). After stirring at RT for 27 h, 50 ml of 20% citric acid were added and the mixture was stirred for 1 h. After adding DCM (100 ml), the DCM phase was removed, dried and concentrated. The residue was dissolved in acetonitrile (100 ml), and 2 N sulfuric acid (20 ml) was added to the solution. After stirring at RT for 24 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 (80 g cartridge, n-heptane/EA gradient of 0-60% within 40 min). 866 mg of the title compound were obtained. LC-MS rt: 1.69 min [M+H]+: 410.0 (met. a)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198272B2
Source datasetuspto-grants-2012_06
ORD IDord-bb4bd5f2485046b692a7bd20f8a2fca7
Source noteuspto-grants-2012_06