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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916721Generated: October 23, 2026

Triethylamine → HCID 69076337, compound

https://huagongshe.com/en/reaction/1916721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Reactant3-(5-Bromopyridin-2-yl)prop-2-yn-1-olHCID 13979730—
Reactantp-Chlorophenylboric acidHCID 17810664—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 69076337HCID 69076337—

Reaction Conditions

Temperature60 °C

Reaction Steps

Under an N2 atmosphere 1 mL (7.22 mmol) triethylamine, 23 mg (0.1 mmol) Pd(OAc)2 and 57.5 mg (0.19 mmol) biphenyl-2-yl-di-tert-butyl-phosphane are added to a solution of 500 mg (2.36 mmol) 3-(5-bromo-pyridin-2-yl)-prop-2-yn-1-ol and 600 mg (3.72 mmol) 4-chlorophenyl-boric acid in 10 mL DMF and 2.5 mL water and the reaction mixture is stirred for 8 h at 60° C. Then 400 mg (2.48 mmol) 4-chlorophenyl-boric acid are added and the mixture is stirred for a further 19 h at 60° C. The mixture is evaporated down i. vac., the residue is combined with 10 mL water and 10 mL EtOAc, the aqueous phase is saturated with NaCl, the organic phase is separated off and dried over Na2SO4. After the desiccant and solvent have been eliminated the residue is purified by chromatography (silica gel, cyc/EtOAc3 2:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618132B2
Source datasetuspto-grants-2013_12
ORD IDord-e96886e555c64fa6a9d8e7dd566e04f0
Source noteuspto-grants-2013_12