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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1386730Erstellt: 26. Oktober 2026

Benzyl Bromide → 4-Bromo-2,6-difluoro-1-(benzyloxy)benzene

https://huagongshe.com/reaction/1386730

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
Edukt4-Bromo-2,6-difluorophenolHCID 2736292—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Bromo-2,6-difluoro-1-(benzyloxy)benzeneHCID 1420764188%

Reaktionsschritte

To a solution of 5.0 g (24.0 mmol) of 2,6 difluoro-4-bromophenol in 20 ml of DMF at rt was added 5 g (36.0 mmol) of K2CO3 followed by 4.5 g (26.3 mmol) of benzyl bromide. The mixture was stirred for 12 h, diluted with H2O, the organic phase washed with sat'd NaCl, and the aqueous phase was then extracted 3× with CH2Cl2. The combined organic layers were dried over Na2SO4 and concentrated. Flash chromatography with a gradient of 0-15% ethyl acetate/hexanes (v/v) afforded 6.3 g (88%) of the title compound: 1H NMR (500 MHz) δ 5.17 (s, 21), 7.06-7.11 (2H). 7.34-7.45 (5H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06265434B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-9e9b5ae7fe764c8692f1ec077e33a89d
Quellennotizuspto-grants-2001_07