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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851356Generated: November 2, 2026

Ethanol → ethyl 7-amino-1-(methoxymethyl)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1851356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactantethyl 1-(methoxymethyl)-7-nitro-1H-indole-2-carboxylateHCID 57475941—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuranHCID 8028—
Productethyl 7-amino-1-(methoxymethyl)-1H-indole-2-carboxylateHCID 5747594491.6%

Reaction Steps

A mixture of ethyl 1-(methoxymethyl)-7-nitro-1H-indole-2-carboxylate (2.35 g), 10% palladium-carbon (0.24 g), ethanol (4 ml) and tetrahydrofuran (10 ml) was stirred at room temperature overnight under a hydrogen atmosphere. Palladium-carbon was filtered off, and the filtrate was concentrated. The residue was subjected to silica gel column chromatography and the title compound (1.92 g, yield 91%) was obtained as a yellow oil from a fraction eluted with ethyl acetate-hexane (1:3, volume ratio).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-28f1df9d6b03483d80dadf5d6ad23ada
Source noteuspto-grants-2015_02