Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459592Generated: October 31, 2026

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

https://huagongshe.com/reaction/1459592

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 numberUS05854262
Source datasetuspto-grants-1998_12
ORD IDord-e942614fc02a4e90952325150c3dc02a
Source noteuspto-grants-1998_12