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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396122Generated: October 30, 2026

Benzyl Bromide → HCID 15000227, compound

https://huagongshe.com/reaction/396122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Hydroxy-2-nitrobenzaldehydeHCID 586137—
SolventDimethylformamideHCID 6228—
ProductHCID 15000227HCID 1500022799.4%

Reaction Steps

8.51 g (61.57 mmol) of potassium carbonate are added to a solution of 10.0 g (58.64 mmol) of 4-hydroxy-2-nitrobenzaldehyde in 70 ml of DMF. The solution is briefly stirred, then 10.53 g (61.57 mmol) of benzyl bromide are added and the reaction mixture is stirred at room temperature for 3 h. The resulting solid is then filtered off, 250 ml of water are added to the filtrate and the aqueous phase is extracted 3× with ethyl acetate. The organic phase is washed twice with water, dried over sodium sulphate, concentrated in vacuo and the residue is dried. 15.0 g (99%) of 4-benzyloxy-2-nitrobenzaldehyde are obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608049B2
Source datasetuspto-grants-2003_08
ORD IDord-f540cf9a013244a58f7effce7f6193f4
Source noteuspto-grants-2003_08