Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010682Generated: October 30, 2026

Benzyl Bromide → HCID 14784149, compound

https://huagongshe.com/reaction/1010682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-5-nitrophenolHCID 10488984—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 14784149HCID 1478414991%

Reaction Steps

To an ice-cold solution of 3-bromo-5-nitro-phenol (21.0 g, 96.33 mmol) in acetone (420.0 mL) was added K2CO3 (40.0 g, 289.41 mmol) followed by addition of benzyl bromide (17.20 mL, 144.40 mmol). The resulting reaction mixture was stirred at room temperature for 2 h. The reaction mixture was then diluted with water and extracted with EtOAc (3×250.0 mL). The combined organics was dried over anhydrous Na2SO4 and concentrated under reduced pressure. The crude was purified over silica gel (100-200 M, 5% EtOAc-Hexane) to get the desired product (27.0 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977340B2
Source datasetuspto-grants-2011_07
ORD IDord-ff08803fcabb4f589fe9e7ca45a5448e
Source noteuspto-grants-2011_07