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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272209Generated: October 26, 2026

Ethanol → 2-Methyl-1-[7-(benzyloxy)indol-3-yl]prop-2-ylamine

https://huagongshe.com/reaction/1272209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3-(2-Methyl-2-nitropropyl)-7-(benzyloxy)indoleHCID 22014778—
CatalystNickelHCID 935—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-1-[7-(benzyloxy)indol-3-yl]prop-2-ylamineHCID 22014779—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 3-(2-methyl-2-nitropropyl)-7-(benzyloxy)indole (25.0 g, 77.1 mmol), Raney Nickel® (9.5 g wet lump), and 3A ethanol (250 mL) is pressurized to 50 psig with H2 and is heated to 60° C. After 1 hour, the mixture is cooled to ambient temperature. The mixture is diluted with tetrahydrofuran (100 mL) and is warmed to 50° C. The catalyst is removed by filtration and the cake is rinsed with 50° C. tetrahydrofuran (4×50 mL). The filtrate is concentrated to a solid which is dried in a 50° C. vacuum oven to provide 22.41 (99%) of 2-methyl-1-[7-(benzyloxy)indol-3-yl]prop-2-ylamine. MS (ES+) m/z 295 (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208505B2
Source datasetuspto-grants-2007_04
ORD IDord-66fe8ead5ffa4e0aba745f09a26647ef
Source noteuspto-grants-2007_04