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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012311Generated: October 27, 2026

Water → 4-(Benzyloxy)-1-iodo-2-nitrobenzene

https://huagongshe.com/reaction/1012311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Iodo-3-nitrophenolHCID 2733454—
SolventAcetoneHCID 180—
Product4-(Benzyloxy)-1-iodo-2-nitrobenzeneHCID 12180180—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 4-iodo-3-nitrophenol (5.00 g, 18.9 mmol) in acetone (50 ml) were added potassium carbonate (3.39 g, 24.6 mmol) and benzyl bromide (2.92 ml, 24.6 mmol), and the mixture was stirred at 50° C. for 6 hr. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under reduced pressure to give 4-benzyloxy-1-iodo-2-nitrobenzene. The obtained crude product (6.20 g) was used for Step 2 without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977331B1
Source datasetuspto-grants-2011_07
ORD IDord-5d29d6383ad14dcab6f7910ed8153512
Source noteuspto-grants-2011_07