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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177339Generated: November 1, 2026

Pyridine → 3,4-Dihydroxy-5-nitrobenzaldehyde

https://huagongshe.com/reaction/1177339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant5-NitrovanillinHCID 81134—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventEthyl AcetateHCID 8857—
Product3,4-Dihydroxy-5-nitrobenzaldehydeHCID 574895767.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a vigorously stirred suspension of 4-hydroxy-3-methoxy-5-nitrobenzaldehyde (47.0 g, 238 mmol) in EtOAc (450 mL) at room temperature, anhydrous aluminum chloride (38.1 g, 286 mmol) was added in one portion. Then pyridine (77 mL, 954 mmol) was added drop wise at 45-50° C. for 30 min. The reaction mixture was refluxed for 2 h and allowed to cool down to 60° C. The reaction mixture was carefully poured into ice/concentrated HCl mixture (265 mL). After stirring at 50° C. for 1 h, the reaction mixture was cooled to 0° C. The formed precipitate was separated by filtration, washed with water, and vacuum-dried to afford the desired compound (29.4 g, 161 mmol, 67.3% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842713B2
Source datasetuspto-grants-2010_11
ORD IDord-4254f67aa7324f78bd491a169b275b99
Source noteuspto-grants-2010_11