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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578771Generated: November 1, 2026

Benzyl Bromide → 2-Chloro-5-(phenylmethoxy)benzenamine

https://huagongshe.com/reaction/578771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-3-nitrophenolHCID 69127—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2-Chloro-5-(phenylmethoxy)benzenamineHCID 20649376—

Reaction Steps

4-Chloro-3-nitrophenol (0.13 g) was dissolved in N,N-dimethylformamide (3 mL). To the solution were added potassium carbonate (0.31 g) and benzyl bromide (0.14 mL), and the mixture was stirred at room temperature for 2 hours. The reaction mixture was diluted with diethyl ether, and the resulting mixture was washed with water and brine successively, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was dissolved in tetrahydrofuran (3 mL). To the solution were added methanol (3 mL), nickel(II) bromide (8 mg) and sodium borohydride (85 mg) under ice-cooling, and the mixture was stirred at the same temperature for 30 minutes. Then the mixture was stirred at room temperature for 30 minutes. The reaction mixture was diluted with ethyl acetate, and the resulting mixture was washed with a saturated aqueous sodium hydrogen carbonate solution, water and brine successively, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to give the title compound (0.15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040693B2
Source datasetuspto-grants-2015_05
ORD IDord-f55622d2f00a42e2b791f956a7f8379a
Source noteuspto-grants-2015_05