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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666233Generated: October 31, 2026

Benzyl Bromide → 4-Benzyloxy-3-chloroaniline

https://huagongshe.com/reaction/1666233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantNitrofunginHCID 12074—
SolventDimethylformamideHCID 6228—
Product4-Benzyloxy-3-chloroanilineHCID 126828573%

Reaction Steps

In a 250 mL flask equipped with a reflux condenser, 2-chloro-4-nitrophenol 4.65 g (26.6 mmol), benzyl bromide 2.97 mL (27.0 mmol, 1 eq), K2CO3 9.4 g (54 mmol, 2 eq) and DMF (60 mL) were added and then heated to reflux. The procedure was conducted as Example 1, the residue was purified by column chromatography to obtain the title compound as brown solid, total yield: 73%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044063B2
Source datasetuspto-grants-2011_10
ORD IDord-8517173762084ce3836e73539789a259
Source noteuspto-grants-2011_10