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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166942Generated: October 26, 2026

2-Methylfuran → N-[5-(2-methyl-5-furyl)thiophene-2-sulfonyl]pyrrole

https://huagongshe.com/reaction/1166942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylfuranHCID 10797—
ReactantN-(5-bromothiophenesulfonyl)pyrroleHCID 23445587—
ReactantHCID 178418306HCID 178418306—
CatalystZincchlorideHCID 3007855—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTetrahydrofuranHCID 8028—
ProductN-[5-(2-methyl-5-furyl)thiophene-2-sulfonyl]pyrroleHCID 2299848119.3%

Reaction Conditions

Temperature-10 °C

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 0.5 M 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613804B2
Source datasetuspto-grants-2003_09
ORD IDord-029f9c10e8a646d5828292a2c68b0e86
Source noteuspto-grants-2003_09