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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613562Generated: October 30, 2026

6-Nitro-m-toluidine → Isopropylidene (5-methyl-2-nitroanilino)methylenemalonate

https://huagongshe.com/reaction/613562

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Nitro-m-toluidineHCID 11356—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
ReactantEthyl orthoformateHCID 31214—
SolventEthanolHCID 702—
ProductIsopropylidene (5-methyl-2-nitroanilino)methylenemalonateHCID 5370557375.5%

Reaction Steps

To a stirred suspension of 5-methyl-2-nitroaniline (10.0 g) in ethanol (20 ml) were added 2,2-dimethyl-1,3-dioxane-4,6-dione (9.95 g) and triethyl orthoformate (10.7 g) at 50° C. The resulting mixture was heated at 120° C. for one hour during which time ethanol (20 ml) was added to the mixture and ethanol liberated was distilled off. After cooling, ethyl acetate (40 ml) was added thereto and the resulting precipitate was collected by filtration. The solid was washed with hot ethanol (40 ml) and allowed to cool to ambient temperature. The precipitate was collected by filtration and air-dried to afford isopropylidene (5-methyl-2-nitroanilino)methylenemalonate (15.2 g) as yellow needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008230
Source datasetuspto-grants-1999_12
ORD IDord-caf00fac7d5440259ad637ff373070c2
Source noteuspto-grants-1999_12