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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51571Generated: October 26, 2026

Triethylamine → 4-Bromo-2-methoxy-1-phenoxy-benzene

https://huagongshe.com/reaction/51571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenylboronic AcidHCID 66827—
Reactant5-Bromo-2-methoxyphenolHCID 142228—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
Product4-Bromo-2-methoxy-1-phenoxy-benzeneHCID 2273628212%

Reaction Steps

A mixture of 4-bromoguaiacol (2.23 g, 11 mmol), phenyl boronic acid (4.03 g, 33 mmol), copper(II) acetate (2.18 g, 12 mmol) and 4A powdered molecular sieves (20 g) in dichloromethane (100 mL) was treated with triethylamine (5.5 g, 55 mmol) then stirred at ambient temperature for 20 hours. The mixture was filtered, concentrated under reduced pressure and purified by flash chromatography on silica gel using heptane/ethyl acetate (75:25) as an eluent to give 4-bromo-2-methoxy-1-phenoxybenzene (350 mg, 12%): 1H NMR (DMSO-d6, 400 MHz) δ 7.3-7.4(m, 3H), 7.15(d, 1H), 7.05(t, 1H), 6.98(d, 1H), 6.85 (d, 2H), 3.77(s, 3H); RP-HPLC (Hypersil HS, 5 μm, 100 A, 4.6×250 mm; 25%-100% acetonitrile—0.05 M ammonium acetate over 10 min, 1 ml/min) tr 13.12 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713474B2
Source datasetuspto-grants-2004_03
ORD IDord-f7c71ebe2db44a70b5b01be8c159771c
Source noteuspto-grants-2004_03