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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447747Generated: October 29, 2026

Sodium Hydroxide → 2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)ethanol

https://huagongshe.com/reaction/447747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantethyl 2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)acetateHCID 20761741—
SolventTetrahydrofuranHCID 8028—
Product2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)ethanolHCID 5781440584%

Reaction Steps

A solution of ethyl 2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)acetate (0.22 g, 1.00 mmol) in THF anh. is added slowly over a suspension of AlLiH4 (0.1 g, 2.63 mmol) in THF anh. (10 mL) cooled in an ice bath. The mixture is maintained under stirring at room temperature for 1 hour and then is refluxed for 3 hours. The mixture is hydrolyzed with ice and NaOH (10%), filtered and the solvent is evaporated under reduced pressure. The residue is dissolved in ethyl acetate and washed with water. The organic phase is removed at reduced pressure and the resulting crude is purified by column chromatography, giving 2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)ethanol (0.15 g, 0.84 mmol, 84%, oil). 1H NMR (300 MHz, CDCl3): δ 1.37 (m, 1H), 1.68 (m, 3H), 1.92 (m, 3H), 2.49 (m, 2H), 2.78 (m, 1H), 3.46 (s, 3H), 3.81 (m, 2H), 5.99 (d, J=2.5 Hz, 1H), 6.50 (d, J=2.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481567B2
Source datasetuspto-grants-2013_07
ORD IDord-f59fcd899c364e788a61ae3c05ede5c1
Source noteuspto-grants-2013_07