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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 3-(3-Hydroxypropyl)-1H-indole-5-carbonitrile | HCID 22405711 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | 5-(Aminomethyl)-1H-indole-3-propanol | HCID 22405693 | 131.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05521188 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-2a496e94b60f41c2a445ee8ebc4f89ac |
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| Source note | uspto-grants-1996_05 |
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