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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818002Generated: October 31, 2026

Benzyl Bromide → 2-Benzyloxy-6-nitroaniline

https://huagongshe.com/reaction/1818002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Amino-3-NitrophenolHCID 4115495—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Benzyloxy-6-nitroanilineHCID 3783741—

Reaction Steps

A mixture of 2-amino-3-nitro-phenol (1.54 g, 0.01 mol), benzyl bromide (1.71 g, 0.01 mol) and K2CO3 (1.54 g, 0.011 mol) in DMF (5.0 mL) was stirred at room temperature. After 20 h, reaction mixture was diluted with water (100 mL) and extracted with EtOAc (100 mL×3). Combined organic layers were washed with 2N NaOH (20 mL×3), water (100 mL), brine (100 mL), dried over anhydrous sodium sulfate and concentrated to afford 2-Benzyloxy-6-nitro-phenylamine, I-107 (2.01 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598397B2
Source datasetuspto-grants-2009_10
ORD IDord-c683b08fc5054cff8aa0f249c122026a
Source noteuspto-grants-2009_10