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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272217Generated: November 3, 2026

Aluminium lithium hydride → 7-benzyloxy-3-(2-aminopropyl)-1H-indole

https://huagongshe.com/reaction/1272217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
Reactant7-benzyloxy-3-(2-nitroprop-1-enyl)-1H-indoleHCID 69517914—
SolventTetrahydrofuranHCID 8028—
Product7-benzyloxy-3-(2-aminopropyl)-1H-indoleHCID 11150198—

Reaction Conditions

Temperature30 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208505B2
Source datasetuspto-grants-2007_04
ORD IDord-2a798c7d05e74db397319a4cb95a0b73
Source noteuspto-grants-2007_04