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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)acetate | HCID 20761741 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(1-methyl-4,5,6,7-tetrahydro-1H-indol-4-yl)ethanol | HCID 57814405 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481567B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-f59fcd899c364e788a61ae3c05ede5c1 |
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| Source note | uspto-grants-2013_07 |
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