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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746747Generated: October 30, 2026

Chlorosulfonic acid → 4-(2-Oxoimidazolidin-1-yl)benzene-1-sulfonyl chloride

https://huagongshe.com/reaction/746747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantHCID 58664909HCID 58664909—
SolventCarbon TetrachlorideHCID 5943—
Product4-(2-Oxoimidazolidin-1-yl)benzene-1-sulfonyl chlorideHCID 21429035—

Reaction Steps

To 1.5 mL (23.1 mmol) of chlorosulfonic acid in 3 mL of carbon tetrachloride at 0° C. was added slowly 500 mg (3.1 mmol) of the compound of Step 1. The reaction was almost completed after 2 h at 0° C. The reaction mixture was poured into ice water slowly, then filtered to collect the solids formed. The aqueous layer was extracted with chloroform (3×100 ml), and the combined organic layers were dried over sodium sulfate, filtered, concentrated in vacuo. The filtered solid and the crude material from the extraction were combined to provide the title compound (LC/MS found: 261.1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393873B2
Source datasetuspto-grants-2008_07
ORD IDord-e4065a2568f149a8887165f4b43e54db
Source noteuspto-grants-2008_07