Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234452Generated: October 31, 2026

Piperidine → HCID 22998462, compound

https://huagongshe.com/reaction/234452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant3,3-Dimethyl-1-butyneHCID 13512—
ReactantN-(5-bromothiophenesulfonyl)pyrroleHCID 23445587—
CatalystCopper iodideHCID 83717—
SolventWaterHCID 962—
ProductHCID 22998462HCID 2299846270.3%

Reaction Steps

A mixture of N-(5-bromothiophene-2-sulfonyl)pyrrole (600 mg, 2.05 mmol), 3,3-dimethyl-1-butyne (338 mg, 4.1 mmol), copper iodide (39 mg, 0.21 mmol), tetrakistriphenylphosphine palladium [Pd(PPh3)4 ] (118 mg, 0.1 mmol) and piperidine (5 ml) was stirred at room temperature for a period of 24 hours under a nitrogen atmosphere. The mixture was then diluted with water (10 ml) and extracted with 3×25 ml portions of ether. The combined ether extracts are washed with brine and dried over MgSO4. The solvent was removed under reduced pressure and crude product purified by column chromatography using 2% ethyl acetate/hexanes to give 423 mg N-[5-(3,3-dimethylbutyn-1-yl)thiophene-2-sulfonyl]pyrrole as a yellow powder (70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594021
Source datasetuspto-grants-1997_01
ORD IDord-73fd03291c794b4885c460f937eae65b
Source noteuspto-grants-1997_01