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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267327Generated: November 1, 2026

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

https://huagongshe.com/reaction/2267327

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 numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-5a9436edb70345df8fd366d6aa68a29a
Source noteuspto-grants-2010_12