HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8097Generated: October 28, 2026
Aluminium lithium hydride → 7-benzyloxy-3-(2-aminopropyl)-1H-indole
https://huagongshe.com/reaction/8097
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 7-benzyloxy-3-(2-nitroprop-1-enyl)-1H-indole | HCID 69517914 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-benzyloxy-3-(2-aminopropyl)-1H-indole | HCID 11150198 | — |
Reaction Steps
Lithium aluminum hydride (LAH, 24 g, 600 mmol) is added portionwise to dry tetrahydrofuran (1800 mL) at −5° C. to 5° C. A solution of the nitroolefin from above (61.6 g, 200 mmol) in tetrahydrofuran (1200 mL) is added to the LAH solution over 30 minutes while maintaining the temperature at −5° C. to 5° C. When the addition is complete, the reaction mixture is allowed to warm to 30° C. over 1.5 hours and is stirred at 25° C. to 35° C. for 2 hours. To complete the reaction, the mixture is heated to 60° C. for 30 minutes. After cooling to 0° C., the reaction is quenched by the sequential addition of water (30 mL), 5 N NaOH (30 mL), and water (100 mL) and the resulting mixture is stirred over the weekend. The aluminum salts are removed by filtration and the cake rinsed with tetrahydrofuran (500 mL). The combined filtrates are concentrated to give 47.6 g (55% purity corrected yield, approx 65% pure) of 7-benzyloxy-3-(2-aminopropyl)-1H-indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087635B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-d323c67d08ed4629b72f93d0bf5352fc |
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| Source note | uspto-grants-2006_08 |
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