HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738518Generated: October 26, 2026
2-Methylfuran → N-[5-(2-methyl-5-furyl)thiophene-2-sulfonyl]pyrrole
https://huagongshe.com/reaction/1738518
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylfuran | HCID 10797 | — |
| Reactant | N-(5-bromothiophenesulfonyl)pyrrole | HCID 23445587 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[5-(2-methyl-5-furyl)thiophene-2-sulfonyl]pyrrole | HCID 22998481 | 19.3% |
Reaction Steps
t-BuLi (1.7 m solution in hexane, 7.9 ml, 14.6 mmol) was added dropwise under constant stirring under a nitrogen atmosphere to a solution of 2-methylfuran (1.0 g, 12 mmol) in THF (20 ml) at -78° C. The solution was then warmed to -10° C. and stirring continued for 45 min. The solution was then added to a solution of zinc chloride (27 ml of a 0.5M solution in THF) at -30° C. and then warmed to room temperature where stirring continued for 1 hr. resulting in a pale yellow clear solution. The solution was then transferred via a steel canula under nitrogen to a solution of N-(5-bromothiophene-2-sulfonyl)pyrrole (Example 33A, 3.5 g, 12 mmol) and tetrakis(triphenylphosphine)-palladium (0) (693 mg, 0.6 mmol) in THF (15 ml) at -78° C. The solution was then warmed to room temperature and stirred for a period of 2 hours. Purification by column chromatography using 2% ethyl acetate gave 680 mg of N-[5-(2-methyl-5-furyl)thiophene-2-sulfonyl]pyrrole as a pale yellow powder (19% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05962490 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-b302f5f0bb9544ca9c77f200d6ef7822 |
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| Source note | uspto-grants-1999_10 |
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