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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459126Generated: November 3, 2026

4-Nitrobenzyl bromide → HCID 85738246, compound

https://huagongshe.com/reaction/1459126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzyl bromideHCID 66011—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Hydroxy-3-methoxy-5-nitrobenzaldehydeHCID 307886—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 85738246HCID 8573824670%

Reaction Conditions

Temperature100 °C

Reaction Steps

5.0 g (1.0 equivalent) of 3-methoxy-5-nitrosalicylaldehyde and 6.03 g (1.1 equivalents) of p-nitrobenzyl bromide were dissolved in 15 ml of 1,4-dioxane, and then 13.5 g (3.5 equivalents) of 1,8-diazabicyclo[5.4.0]undeca-7-ene was added thereto. The resulting mixture was heated at about 100° C. for three hours with stirring, and then cooled to room temperature. Thereafter, the resulting solid substance was filtered off and sufficiently washed with ethanol. Thus, 4.55 g of 2-(p-nitrophenyl)-5-nitro-7-methoxybenzo[b]furan was obtained (yield: 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05853930
Source datasetuspto-grants-1998_12
ORD IDord-c9a9a0a4cd594046bd5a44e768142206
Source noteuspto-grants-1998_12