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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468432Generated: November 2, 2026

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

https://huagongshe.com/reaction/468432

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 numberUS08623905B2
Source datasetuspto-grants-2014_01
ORD IDord-33db963813cb415e92205dc8bf4b21c5
Source noteuspto-grants-2014_01