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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696121Generated: November 1, 2026

Chlorosulfonic acid → 4-(1-(2,2,2-Trifluoroacetyl)piperidin-4-yl)benzene-1-sulfonyl chloride

https://huagongshe.com/reaction/1696121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantHCID 18348438HCID 18348438—
SolventEthyl AcetateHCID 8857—
Product4-(1-(2,2,2-Trifluoroacetyl)piperidin-4-yl)benzene-1-sulfonyl chlorideHCID 1797347894%

Reaction Steps

Chlorosulfonic acid (2 mL) was added to 2,2,2-trifluoro-1-(4-phenylpiperidin-1-yl)ethanone (1.0 g, 3.9 mmol) in a single portion, and the reaction was stirred for 20 minutes until gas evolution ceased (exothermic reaction). The solution was poured into a mixture of ice water (200 mL) and EtOAc (20 mL). The organic layer was concentrated and purified via silica gel chromatography using 8/2 hexanes/EtOAc to obtain 4-(1-(2,2,2-trifluoroacetyl)piperidin-4-yl)benzene-1-sulfonyl chloride as a clear oil (1.3 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163720B2
Source datasetuspto-grants-2012_04
ORD IDord-4fc7fb0afc0f43229acdbcc41ff710f5
Source noteuspto-grants-2012_04