Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199937Generated: October 31, 2026

Sodium Hydroxide → 2-{[2-(1H-Indol-3-yl)ethyl]amino}ethan-1-ol

https://huagongshe.com/reaction/1199937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14477069HCID 14477069—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product2-{[2-(1H-Indol-3-yl)ethyl]amino}ethan-1-olHCID 1235713173%

Reaction Conditions

Temperature-10 °C

Reaction Steps

398 g of the product of Step A were dissolved in 4 liters of tetrahydrofuran cooled to +10° C. and while maintaining this temperature, 400 g of 25% sodium diethyl dihydroaluminate in toluene were introduced. The mixture was stirred for 90 minutes while allowing the temperture to rise to 17° C. The medium was cooled to -10° C. and 400 ml of sodium hydroxide solution in 1200 ml of water were introduced over 80 minutes while keeping the temperature at 0° C. during the introduction. The mixture was stirred for 2 hours at +10° C. then allowed to rise to ambient temperature for 16 hours with slower stirring. After decanting, the organic phase was washed with water and the wash water was extracted with ethyl acetate and methylene chloride. The combined organic phases were diluted with methylene chloride and dried, and the solvents were expelled at 40° C. under reduced pressure. The residue was triturated in 1300 ml of ethyl acetate for one hour, separated, washed with ethyl acetate and dried to obtain 240.8 g of the expected product melting at 92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04904655
Source datasetuspto-grants-1990_02
ORD IDord-638f223778ee479590ea575c71e078fd
Source noteuspto-grants-1990_02