HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614675Generated: October 25, 2026
1-Iodopentane → 2-Pentyl-5-(t-butylsulfonamido)thiophene
https://huagongshe.com/reaction/1614675
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Iodopentane | HCID 12335 | — |
| Reactant | 2-(t-Butylsulfonamido)thiophene | HCID 19789655 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Pentyl-5-(t-butylsulfonamido)thiophene | HCID 18938921 | 60% |
Reaction Steps
To a solution of 2-(t-butylsulfonamido)thiophene (3.42 g, 15.6 mmol) in anhydrous THF coole 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05198438 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-3a87e448f60d4a7197645859f090430f |
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| Source note | uspto-grants-1993_03 |
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