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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875487Generated: October 30, 2026

Benzyl Bromide → 4-Benzyloxy-3-chloroaniline

https://huagongshe.com/reaction/1875487

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 numberUS08309563B2
Source datasetuspto-grants-2012_11
ORD IDord-0c179d1f8094463a86e30a4013bc13d9
Source noteuspto-grants-2012_11