Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642634Generated: November 2, 2026

Benzyl Bromide → 3-(Benzyloxy)-4-nitrobenzaldehyde

https://huagongshe.com/reaction/1642634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Hydroxy-4-nitrobenzaldehydeHCID 69712—
SolventWaterHCID 962—
Product3-(Benzyloxy)-4-nitrobenzaldehydeHCID 12111719—

Reaction Steps

To a stirred solution of benzyl bromide (6.9 g, 40.3 mmol) and 3-hydroxy-4-nitrobenzaldehyde (9.7 g, 58.0 mmol) is added K2CO3 (8.9 g, 64.4 mmol). The mixture is stirred at ambient temperature overnight, diluted with water and extracted with EtOAc. The organic phase is washed with aqueous K2CO3 and brine, dried over MgSO4, filtered and concentrated to afford 3-benzyloxy-4-nitrobenzaldehyde as a yellow solid: MS (M+H)+=258.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119666B2
Source datasetuspto-grants-2012_02
ORD IDord-bc8ed470fa644b76912b2e450ab1fffd
Source noteuspto-grants-2012_02