Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454288Generated: October 30, 2026

N-Methyl-5-benzyloxyindole → 1-Methyl-1H-indol-5-ol

https://huagongshe.com/reaction/454288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl-5-benzyloxyindoleHCID 259196—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-Methyl-1H-indol-5-olHCID 1084452597%

Reaction Steps

A solution of 5-benzyloxy-1-methylindole (3.5 g, 15.7 mmol), in ethanol (100 ml) was hydrogenated at ambient temperature and 1 atmosphere pressure hydrogen for 4 hours using 10% palladium on carbon (0.5 g) as catalyst. The catalyst was filtered off and the filtrate evaporated in vacuo. The residue was purified by silica column chromatography eluting with ethyl acetate/dichloromethane (10/90) to give 5-hydroxy-1-methylindole (2.1 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-84a72863aaa846bda8f2d1f2f22ab9f7
Source noteuspto-grants-2013_07