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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 51571Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/51571

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktPhenylboronic AcidHCID 66827—
Edukt5-Bromo-2-methoxyphenolHCID 142228—
KatalysatorCupric acetateHCID 8895—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Bromo-2-methoxy-1-phenoxy-benzeneHCID 2273628212%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713474B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-f7c71ebe2db44a70b5b01be8c159771c
Quellennotizuspto-grants-2004_03