Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840601Generated: October 30, 2026

2-Chloro-5-nitrobenzaldehyde → Benzaldehyde, 2-methoxy-5-nitro-

https://huagongshe.com/reaction/840601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-nitrobenzaldehydeHCID 72933—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductBenzaldehyde, 2-methoxy-5-nitro-HCID 90685—

Reaction Steps

A mixture of 2.5 grams (13.5 mmol) of 2-chloro-5-nitrobenzaldehyde (Aldrich Chem. Co.) in 250 mL of CH3OH was treated with 2.92 grams (54.1 mmol) of sodium methoxide, refluxed for 16 hours and allowed to cool to room temperature. After removal of the solvent in vacuo, the residue was suspended in water, treated with 2N HCl (adjusting to pH<5) and extracted into methylene chloride. After drying over MgSO4, the solvent was removed in vacuo to give a yellow solid, 2.02 grams (83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369074B1
Source datasetuspto-grants-2002_04
ORD IDord-df2cbe0415044cf793849a43e12d4722
Source noteuspto-grants-2002_04