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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127506Generated: October 26, 2026

1H-Indole, 6-methyl- → Alpha-nitro-6-methyl-3-indoleacrylic acid methylester

https://huagongshe.com/reaction/127506

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indole, 6-methyl-HCID 137928—
Reactantalpha-Nitro-beta-ethoxyacrylic acid methylesterHCID 53395203—
ProductAlpha-nitro-6-methyl-3-indoleacrylic acid methylesterHCID 54365062—

Reaction Steps

A mixture of 32.5 g (0.25 mol) of 6-methylindole and 52.5 g (0.30 mol) of α-nitro-β-ethoxyacrylic acid methylester was let stand in a large crystallization dish at room temperature for 20 hours. The brown-orange solid was triturated with ether-hexane 1:1, the crystalline material collected by filtration, washed with ether and dried to afford 44.5 g. (69%) of product as orange crystals, m.p. 167°-169°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256641
Source datasetuspto-grants-1981_03
ORD IDord-e1d95fc4561949359c3640c74721b0b7
Source noteuspto-grants-1981_03