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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918451Generated: October 30, 2026

3-Nitrobenzaldehyde → HCID 68120470, compound

https://huagongshe.com/reaction/918451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
ReactantDiethyl oxalacetateHCID 66951—
ReactantHCID 45122131HCID 45122131—
SolventEthanolHCID 702—
ProductHCID 68120470HCID 68120470—

Reaction Steps

After heating a solution of 15.1 g of 3-nitrobenzaldehyde, 16 g of β-amino-γ-methoxycrotonic acid ethyl ester and 19 g of oxalacetic acid diethyl ester in 60 ml of ethanol under reflux for 12 hours, the mixture is evaporated in vacuo and 2-methoxymethyl-4-(3'-nitrophenyl)-1,4-dihydropyridine-3,5,6-tricarboxylic acid triethyl ester is obtained in almost quantitative yield, in the form of a yellow oil (nD50 =1.5353).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03971796
Source datasetuspto-grants-1976_07
ORD IDord-9ffe6339e7ca4879a6e53c4c63383e53
Source noteuspto-grants-1976_07