Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274431Generated: October 26, 2026

Hydrogen Bromide → 3,4-Dihydroxy-5-nitrobenzaldehyde

https://huagongshe.com/reaction/274431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant5-NitrovanillinHCID 81134—
SolventDichloromethaneHCID 6344—
Product3,4-Dihydroxy-5-nitrobenzaldehydeHCID 5748957—

Reaction Steps

17.1 g of 4-hydroxy-3-methoxy-5-nitrobenzaldehyde are treated with 170 ml of constant-boiling hydrobromic acid and heated under reflux for 3.5 hours. After cooling the separated precipitate is filtered under suction, washed twice with ice-water and taken up in ethyl acetate. The organic phase is washed twice with 50 ml of sodium chloride solution each time, dried over magnesium sulfate and evaporated in a water-jet vacuum. The crystals obtained are taken up in methylene chloride, whereupon the solution is filtered over a ten-fold amount of silica gel. The material obtained is crystallized from ethyl acetate/isopropyl ether. There is obtained 3,4-dihydroxy-5-nitrobenzaldehyde in the form of yellow crystals of m.p. 142°-143°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389653
Source datasetuspto-grants-1995_02
ORD IDord-abb4814a8f9b43979a8172da63570498
Source noteuspto-grants-1995_02