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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441437Generated: November 2, 2026

Benzyl Chloride → 1-(Benzyloxy)-4-bromo-2-nitrobenzene

https://huagongshe.com/reaction/1441437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-nitrophenolHCID 24364—
SolventDimethylformamideHCID 6228—
Product1-(Benzyloxy)-4-bromo-2-nitrobenzeneHCID 11278242100%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-Bromo-2-nitro-phenol (Aldrich, 2.18 g, 10 mmol) was treated with K2CO3 (Aldrich, 2.76 g, 20 mmol) in DMF (Aldrich, 100 mL) at ambient temperature for 20 min. Benzyl chloride (Aldrich, 1.52 g, 12 mmol) was added. The mixture was stirred at 100° C. for 6 h. It was then poured into ice/water (200 mL) and stirred at ambient temperature for 10 hours. The white solid was filtered and dried to give the title compound (3.0 g, yield, 100%). 1H NMR (300 MHz, CDCl3) δ 5.23 (s, 2H), 7.01 (d, J=9.2 Hz, 1H), 7.31-7.49 (m, 5H), 7.58 (dd, J=9.0, 2.5 Hz, 1H), 7.98 (d, J=2.7 Hz, 1H) ppm. MS (DCI/NH3): 325 (M+H)+, 327 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655657B2
Source datasetuspto-grants-2010_02
ORD IDord-8dfc4a8708324e998f1b8975aa6ee775
Source noteuspto-grants-2010_02