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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70502Generated: October 25, 2026

Bromide ion → HCID 67396867, compound

https://huagongshe.com/reaction/70502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl 5-bromopicolinateHCID 12686158—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418476HCID 178418476—
ProductHCID 67396867HCID 6739686787%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of zinc chloride (27 g) in tetrahydrofuran (300 mL) was cooled to 0° C. in the presence of a nitrogen gas, and a 1 M solution of cyclopropanemagnesium bromide in tetrahydrofuran (186 mL) was added thereto, followed by stirring at room temperature for 30 minutes. The reaction solution was cooled to 0° C. Dichlorobis(triphenylphosphine)-palladium(II) (3.26 g) and a solution of ethyl 5-bromopyridine-2-carboxylate (21.4 g) in tetrahydrofuran (100 mL) were sequentially added, and the mixture was stirred at 0° C. for 30 minutes and at room temperature for one hour. The reaction solution was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered. The solvent was then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1→1:1) to give ethyl 5-cyclopropylpyridine-2-carboxylate (15.5 g, 87%) as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822503B2
Source datasetuspto-grants-2014_09
ORD IDord-e01d7efd5981461e9c5e56bb7c6eb516
Source noteuspto-grants-2014_09