Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41055Generated: October 26, 2026

(+/-)-3-(5-ethoxy-1H-indol-3-yl)-2-methyl-2-nitro-propionic acid methyl ester → (+/-)-2-amino-3-(5-ethoxy-1H-indol-3-yl)-2-methyl-propionic acid methyl ester

https://huagongshe.com/reaction/41055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+/-)-3-(5-ethoxy-1H-indol-3-yl)-2-methyl-2-nitro-propionic acid methyl esterHCID 86634329—
SolventMethanolHCID 887—
Product(+/-)-2-amino-3-(5-ethoxy-1H-indol-3-yl)-2-methyl-propionic acid methyl esterHCID 6885152190%

Reaction Steps

To a stirred solution of (+/−)-3-(5-ethoxy-1H-indol-3-yl)-2-methyl-2-nitro-propionic acid methyl ester (5.3 g, 17.3 mmol) in dry methanol (50 ml) Raney nickel is added and the mixture is stirred at room temperature under H2 at atmospheric pressure overnight. The reaction mixture is filtered through a pad of Celite and the solid is washed with methanol. The filtrate is concentrated and the residue is purified by column chromatography (dichloromethane-methanol, 95:5) to give (+/−)-2-amino-3-(5-ethoxy-1H-indol-3-yl)-2-methyl-propionic acid methyl ester (4.2 g, 90%) as a white crystals. M.p. 165-166° C. (from ethyl acetate-hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530493B2
Source datasetuspto-grants-2013_09
ORD IDord-512f4907283b4e5f8a469848b2c4ebb9
Source noteuspto-grants-2013_09