Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043106Generated: November 2, 2026

Chlorosulfonic acid → HCID 59465632, compound

https://huagongshe.com/reaction/2043106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantHCID 839837HCID 839837—
ProductHCID 59465632HCID 5946563272%

Reaction Conditions

Temperature155 °C

Reaction Steps

A mixture of 2,2,2-trifluoro-1-(4-phenylpiperazin-1-yl)ethanone (1.0 g, 3.9 mmol) and chlorosulfonic acid (6 mL) was heated at 155° C. for 15 min. After cooling to RT, the mixture was poured into ice water and extracted with EtOAc. The organic layer was concentrated and purified via silica gel chromatography using 7/3 hexanes/EtOAc to obtain 4-(4-(2,2,2-trifluoroacetyl)piperazin-1-yl)benzene-1-sulfonyl chloride as a yellow solid (1.0 g, 72%). 1H NMR (400 MHz, CDCl3) δ 7.93-7.89 (m, 2H), 6.96-6.92 (m, 2H), 3.88 (t, J=5.3 Hz, 2H), 3.83 (t, J=5.1 Hz, 2H), 3.55-3.52 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586589B2
Source datasetuspto-grants-2013_11
ORD IDord-bf01504a1b6d4636afc499d34b3e01fc
Source noteuspto-grants-2013_11