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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747494Generated: October 31, 2026

Ammonium Chloride → HCID 29997195, compound

https://huagongshe.com/reaction/1747494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
Reactant2-Bromo-5-chloropyridineHCID 817098—
ReactantSodium t-butoxideHCID 23676156—
Reactant(+/-)-2,2-Bis(diphenylphosphino)-1,1-binaphthylHCID 86595863—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 29997195HCID 2999719553%

Reaction Steps

Sodium t-butoxide (1.25 g, 13.0 mmol), 2,2-bis(diphenylphosphino)-1,1-binaphthyl (0.485 g, 0.779 mmol), and tris(dibenzylideneacetone)dipalladium(0) (0.238 g, 0.260 mmol) were added to a solution of ethyl piperidine-4-carboxylate (2.00 g, 10.4 mmol) and 2-bromo-5-chloropyridine (2.00 g, 10.4 mmol) in toluene (50 mL), and the mixture was stirred for 1 hour under heating to reflux. A saturated ammonium chloride aqueous solution was added to the reaction solution, followed by extraction with toluene twice. The obtained organic layer was washed with brine and then dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography [elute: hexane/ethyl acetate=85/15] to obtain the title compound (1.47 g, yield: 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150575B2
Source datasetuspto-grants-2015_10
ORD IDord-97c87c3deac449828209adf81c271355
Source noteuspto-grants-2015_10