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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592730Generated: October 31, 2026

Pyridine → 1-Bromo-2-phenoxy-benzene

https://huagongshe.com/reaction/1592730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-BromophenolHCID 7244—
ReactantPhenylboronic AcidHCID 66827—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
Product1-Bromo-2-phenoxy-benzeneHCID 37483—

Reaction Steps

A mixture of phenylboronic acid (5.12 g, 42 mmol), 2-bromophenol (3.55 g, 21 mmol), Cu(OAc)2 (7.63 g, 42 mmol), pyridine (8 ml, 103 mmol) and 4 Å molecular sieves (2.1 g) in CH2Cl2 was stirred at r.t. overnight. The mixture was diluted with CH2Cl2, filtered through celite, washed with 1M NaOH, brine and dried. Removal of solvent gave 1-bromo-2-phenoxybenzene, crystals (1.40 g, 27%). LRMS (ESI+): 248 (M+1). 1-Bromo-2-phenoxybenzene was coupled to piperazine using the Buchwald chemistry described in preparation 1A to afford the title compound. LRMS (ESI+) 255 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291619B2
Source datasetuspto-grants-2007_11
ORD IDord-c7b8a8945abd4cd89524c85d553cba9a
Source noteuspto-grants-2007_11