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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656122Generated: October 25, 2026

1-Iodopentane → 2-Pentyl-5-(t-butylsulfonamido)thiophene

https://huagongshe.com/reaction/1656122

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodopentaneHCID 12335—
Reactant2-(t-Butylsulfonamido)thiopheneHCID 19789655—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Pentyl-5-(t-butylsulfonamido)thiopheneHCID 1893892160%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution of 2-(t-butylsulfonamido)thiophene (3.42 g, 15.6 mmol) in anhydrous THF cooled to -78° C. under N2 was added 2.5M n-BuLi (15.6 mL, 2.5 equiv). The reaction was warmed to -20° C. over 3.5 h. After stirring at -20° C. for an addional h, iodopentane (2.4 mL, 1.2 equiv) was added. The ice bath was removed and the reaction was stirred at rt overnight. The next day the reaction was quenched with sat'd NH4Cl solution and the THF was removed in vacuo. The residue was extracted with Et2O/EtOAc and washed with water and brine. The organic was dried over anhydrous MgSO4 and concentrated in vacuo. The product was purified by flash chromatography on a silica column eluting with Hex/EtOAc (15:1). Removal of the solvent afforded 2.72 g (60%) of the titled compound as a yellow oil. Rf=0.4 (6:1 Hex/EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05252574
Source datasetuspto-grants-1993_10
ORD IDord-06b1251e0631498d98279cd9bc00e27f
Source noteuspto-grants-1993_10