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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507552Generated: November 3, 2026

Piperidine → 1-[(5-Bromo-2-thienyl)sulfonyl]piperidine

https://huagongshe.com/reaction/507552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTriethylamineHCID 8471—
Reactant5-Bromothiophene-2-sulfonyl chlorideHCID 2733924—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product1-[(5-Bromo-2-thienyl)sulfonyl]piperidineHCID 558610—

Reaction Steps

Piperidine (0.72 g, 8.41 mmol) was added to a solution of 5-bromothiophene-2-sulfonyl chloride (2 g, 7.65 mmol) in tetrahydrofuran (100 mL) at 0° C. followed by triethylamine (0.93 g, 9.18 mmol) added slowly. The resulting mixture was stirred at rt overnight and 100 mL of brine was added. The mixture was extracted with ethyl acetate (3×100 mL). The combined organic layer was washed with brine (100 mL), dried over anhydrous sodium sulfate and filtered. Removal of the solvent gave the title compound as a slightly yellow solid (quantitative yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786132B2
Source datasetuspto-grants-2010_08
ORD IDord-9b41dada967d4a4199718bd66cd3fab5
Source noteuspto-grants-2010_08