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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554263Generated: October 28, 2026

Sodium hydride → HCID 66924958, compound

https://huagongshe.com/reaction/554263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
ReactantSodium BicarbonateHCID 516892—
ReactantPyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
ReactantHCID 52987784HCID 52987784—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66924958HCID 6692495864%

Reaction Steps

Ethyl 5-bromo-2-methyl-1H-pyrrole-3-carboxylate (2.26 g) was dissolved in tetrahydrofuran (100 mL), sodium hydride (60% in oil, 1.16 g) was added and the mixture was stirred at room temperature for 15 min. 15-Crown-5 (5.90 mL) was added and the mixture was further stirred at the same temperature for 15 min, and 3-pyridinesulfonyl chloride hydrochloride (3.13 g) was added. The reaction mixture was stirred at room temperature for 1 hr, saturated aqueous sodium hydrogencarbonate solution was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=19:1→7:3) to give the title compound as a yellow oil (yield 2.31 g, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048909B2
Source datasetuspto-grants-2011_11
ORD IDord-4edc92abb9364c1cb3bc80efc7e0bff7
Source noteuspto-grants-2011_11