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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569043Generated: October 25, 2026

Ethenamine, N,N-dimethyl-2-nitro- → 4-Ethoxycarbonyl-3-(2-nitrovinyl)indole

https://huagongshe.com/reaction/569043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthenamine, N,N-dimethyl-2-nitro-HCID 518458—
ReactantEthyl indole-4-carboxylateHCID 605034—
Solvent2,2,2-Trifluoroethyl AcetateHCID 136256—
Product4-Ethoxycarbonyl-3-(2-nitrovinyl)indoleHCID 54059630—

Reaction Steps

5 g of 4-ethoxycarbonyl indole are added to a solution of 3.1 g of dimethylamino-2-nitroethylene in 20 ml of trifluoroethyl acetate refrigerated under argon. The reaction mixture is introduced into ice water after it had been standing overnight at room temperature. The aqueous phase is repeatedly extracted with ethyl acetate. The combined ethyl acetate extracts are extracted first with sodium bicarbonate solution, then a saturated sodium chloride solution, dried and evaporated. The residue is recrystallized from ethanol. Yield: 4.5 g of 4-ethoxycarbonyl-3-(2-nitrovinyl)-indole. Yellow crystals with a 197°-199° C. melting point.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731358
Source datasetuspto-grants-1988_03
ORD IDord-6f2a0ddab3ef4b25b66fd79945d51302
Source noteuspto-grants-1988_03