Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394341Generated: October 31, 2026

Chlorosulfonic acid → HCID 22676671, compound

https://huagongshe.com/reaction/1394341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
Reactant1-(4-Benzylpiperidin-1-yl)-2,2,2-trifluoroethanoneHCID 897795—
SolventDichloromethaneHCID 6344—
ProductHCID 22676671HCID 2267667141.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 1-(trifluoroacetyl)-4-benzylpiperidine (29.2 g, 108 mmol) and dichloromethane (10 ml) was added dropwise to chlorosulfonic acid (36 ml, 539 mmol) over period of 1 h at −10° C. The mixture was stirred at 0° C. for 1 h and then at room temperature for 1 h. The whole was poured into ice-water (500 ml). The mixture was extracted with dichloromethane (200 ml×2). The extracts were washed with 5% aqueous sodium bicarbonate (500 ml), saturated sodium chloride solution (500 ml) successively. The organic layer was dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography (silica gel 100 g, ethyl acetate/hexane=1/20 to 1/5) to obtain the title compound (16.5 g, 41%) as a colorless crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348324B2
Source datasetuspto-grants-2008_03
ORD IDord-c8e9776333d046daac2860ed335fd16a
Source noteuspto-grants-2008_03