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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659048Generated: October 30, 2026

Nitrogen → HCID 12887440, compound

https://huagongshe.com/reaction/659048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTriethylamineHCID 8471—
Reactant1,4-DioxaneHCID 31275—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
Reactant2-(Dicyclohexylphosphino)biphenylHCID 2734216—
Reactant4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 12887440HCID 12887440—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of compound b (77 g, 0.22 mol), 4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (57 g, 0.44 mol) and Et3N (92 mL, 0.66 mol) in dioxane (500 mL) was purged with N2 for 30 minutes. Then Pd(OAc)2 (2.7 g, 0.011 mol) and biphenyl-2-yl-dicyclohexyl-phosphane (8.5 g, 0.022 mol) were added to the resulting mixture. After the addition, the reaction mixture was stirred at 80° C. for 1.5 hours. TLC (petroleum ether/EtOAc 30:1) indicated complete consumption of compound b. The resulting mixture was washed with saturated NH4Cl (500 mL), H2O (500 mL) and brine (500 mL) in sequence, dried over Na2SO4 and concentrated in vacuo to give crude compound c, which was purified by column chromatography (silica gel, petroleum ether/EtOAc from 5:1 to 1:1) to yield pure compound c (35 g, yield: 45%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080556B2
Source datasetuspto-grants-2011_12
ORD IDord-878b63313df84d4ca0677560d4643b03
Source noteuspto-grants-2011_12