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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184521Generated: October 29, 2026

Water → 7-(3-chloropropoxy)-1H-indole

https://huagongshe.com/reaction/2184521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium hydrideHCID 24758—
Reactant7-HydroxyindoleHCID 2737651—
SolventDimethylformamideHCID 6228—
Product7-(3-chloropropoxy)-1H-indoleHCID 15384964—

Reaction Steps

To a stirred suspension of sodium hydride (0.8 g, 17 mmol of a 50% oil dispersion in dimethylformamide (20 ml), under nitrogen, was added dropwise 7-hydroxyindole (2.1 g, 15.7 mmol) in dimethylformamide (20 ml). After complete addition, the reaction was stirred at ambient temperature for 0.5 hour and then cooled to 15° C. To this cooled solution was added, dropwise, 1-bromo-3-chloropropane (2.5 g, 15.7 mmol) in dimethylformamide (5 ml). The reaction was then stirred at ambient temperature for 16 hours. The reaction was poured into water, and the aqueous suspension extracted with ethyl acetate. The ethyl acetate was washed with water, dried (MgSO4), and the solvent was concentrated to afford a dark brown oil. Following flash chromatography an silica gel. 7-(3-chloropropoxy)indole was obtained as a colorless oil, 1.0 g. ANALYSIS: Calculated for C11H12ClNO: 63.01%C 5.77%H 6.68%,N Found: 63.25%C 5.61%H 6.65%N

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037729E1
Source datasetuspto-grants-2002_06
ORD IDord-5921c3d8e00f422486ce683c020e6413
Source noteuspto-grants-2002_06