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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465460Generated: November 1, 2026

Toluene → HCID 10920688, compound

https://huagongshe.com/reaction/1465460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDiethylamineHCID 8021—
Reactant3-BromopyridineHCID 12286—
ReactantSodium t-butoxideHCID 23676156—
CatalystPalladium, tris[mu-[(1,2-eta:4,5-eta)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]di-, compd. with trichloromethane (1:1)HCID 11029508—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 10920688HCID 1092068836.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a mixture of 4,5-bis(diphenylphosphino)-9,9′-dimethylxanthene (521 mg, 0.90 mmol), tris(dibenzylideneacetone)dipalladium (0)-chloroform adduct (311 mg, 0.30 mmol), sodium t-butoxide (2.16 g, 23 mmol) and anhydrous toluene (37 ml) were added 3-bromopyridine (1.5 ml, 15 mmol) and diethylamine (1.9 ml, 18.0 mmol). The mixture was heated to 70° C., and the mixture was stirred for 3 hrs and at room temperature overnight. Water and ethyl acetate were added to the reaction mixture. The mixture was stirred, stood still and partitioned. The aqueous layer was extracted with ethyl acetate, and the combined organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:1→2:1) to give N,N-diethylpyridin-3-amine (820 mg, yield 36%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999989B2
Source datasetuspto-grants-2015_04
ORD IDord-5c193408bd574d5a95464e31b952091a
Source noteuspto-grants-2015_04