Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441081Generated: November 1, 2026

Methanol → 5-(Aminomethyl)-1H-indole-3-propanol

https://huagongshe.com/reaction/441081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAcetonitrileHCID 6342—
Reactant3-(3-Hydroxypropyl)-1H-indole-5-carbonitrileHCID 22405711—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductAmmonium HydroxideHCID 14923—
Product5-(Aminomethyl)-1H-indole-3-propanolHCID 22405693131.2%

Reaction Steps

To a solution of 5-cyano-3-(3-hydroxypropyl)indole (1.00 g, 0.005 mol) in 30 mL of absolute ethanol was added 10% palladium-on-charcoal (1.00 g) and the mixture was hydrogenated on a Parr shaker at 40 psi for 6 h. The mixture was then filtered, through Celite, the filtercake was washed with additional ethanol and the filtrate was evaporated to give a colourless gum. Flash chromatography (SiO2 /MeCN--MeOH, 9:1 then MeCN--MeOH--NH4OH, 90:9:1) afforded the essentially pure title compound (0.67 g, 70%) as a colourless gum: IR (neat) 3250 cm-1 ; 1H NMR (DMSO-d6, 200 MHz) δ 10.60 (s, 1H), 7.41 (s, 1H), 7.23 (d, J=8.2 Hz, 1H), 7.04 (s, 1H), 7.02 (d, J=8.1 Hz, 1H), 4.4 (br s, 1H), 3.75 (s, 2H), 3.46 (t, J=6.5 Hz, 2H), 3.3 (br s, 2H), 2.68 (m, 2H), 1.78 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521188
Source datasetuspto-grants-1996_05
ORD IDord-2a496e94b60f41c2a445ee8ebc4f89ac
Source noteuspto-grants-1996_05