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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919855Generated: November 2, 2026

Piperidine → 3-(Piperidine-1-sulfonyl)benzoic acid

https://huagongshe.com/reaction/1919855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantBenzoic acid, 3-(chlorosulfonyl)-HCID 77641—
SolventDichloromethaneHCID 6344—
Product3-(Piperidine-1-sulfonyl)benzoic acidHCID 76788990.4%

Reaction Steps

To a stirred solution of 3-(chlorosulfonyl)benzoic acid (1.10 g, 5.00 mmol) in DCM (10 mL) was added piperidine (1.49 g, 17.5 mmol) at 0° C., and the resulting solution stirred for 30 minutes. The volatiles were then removed in vacuo and the residue treated with aqueous 1N KHSO4. The aqueous phase was then extracted with ethyl acetate (×3), and the combined organic phases dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford 3-(piperidin-1-ylsulfonyl)benzoic acid (1.22 g, 4.52 mmol, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168673B2
Source datasetuspto-grants-2012_05
ORD IDord-391a830bf78347ad88d2fef5341f9618
Source noteuspto-grants-2012_05