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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075892Generated: October 30, 2026

Ethyl Acetate → HCID 21540638, compound

https://huagongshe.com/reaction/1075892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 21540629HCID 21540629—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventEthanolHCID 702—
ProductHCID 21540638HCID 21540638—

Reaction Steps

A solution of 24.4 g. (0.09 mole) of N-ethyl-3-methoxy-6-nitro-4-trifluoromethylaniline in 200 ml. of ethyl acetate, plus 100 ml. of ethanol, was hydrogenated in the presence of 0.2 g. of platinum oxide at room temperature. The theoretical amount of hydrogen was absorbed in 19 hours of shaking at 60 psi. The catalyst was removed by filtration and the solvent evaporated at reduced pressure. The solid residue was dissolved in 200 ml. of absolute ethanol and 12.58 g. (0.10 mole) of ethyl methylcarboximidate hydrochloride added. The mixture was stirred overnight at room temperature and the solvent removed at reduced pressure. Trituration of the brown residue with 200 ml. of chloroform, filtration, and evaporation of solvent from the filtrate left the crude residual product. Crystallization from hexane-CCl4 (3:1) gave 18.1 g. (76%) of brown, shiny needles. Recrystallization from hexane gave the pure product, m.p. 127° - 129.5°C. whose structure was confirmed by an NMR spectrum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954788
Source datasetuspto-grants-1976_05
ORD IDord-a33ba4cf0805406d9a3ff97507483b42
Source noteuspto-grants-1976_05