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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503429Generated: November 3, 2026

ethyl 2-(5-nitro-1H-indol-2-yl)propanoate → ethyl 2-(5-amino-1H-indol-2-yl)propanoate

https://huagongshe.com/reaction/503429

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 2-(5-nitro-1H-indol-2-yl)propanoateHCID 59129193—
ReactantTin tetrachloride dihydrateHCID 85782573—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Productethyl 2-(5-amino-1H-indol-2-yl)propanoateHCID 5912945399.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of ethyl 2-(5-nitro-1H-indol-2-yl)propanoate (0.10 g, 0.38 mmol) in ethanol (4 mL) was added tin chloride dihydrate (0.431 g, 1.91 mmol). The mixture was heated in the microwave at 120° C. for 1 h. The mixture was diluted with ethyl acetate before water and saturated aqueous NaHCO3 were added. The reaction mixture was filtered through a plug of celite using ethyl acetate. The organic layer was separated from the aqueous layer. The organic layer was dried over Na2SO4, filtered and evaporated under reduced pressure to give ethyl 2-(5-amino-1H-indol-2-yl)propanoate (0.088 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776905B2
Source datasetuspto-grants-2010_08
ORD IDord-878b212258fe4211bf9e87303f3ea5a1
Source noteuspto-grants-2010_08