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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657939Generated: October 28, 2026

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

https://huagongshe.com/reaction/657939

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076336B2
Source datasetuspto-grants-2011_12
ORD IDord-2b44608ad79449bdaccc069942e0bbfc
Source noteuspto-grants-2011_12