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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50994Generated: October 25, 2026

Indole → 1-(3-Chloropropyl)-1H-indole

https://huagongshe.com/reaction/50994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium HydroxideHCID 14797—
SolventDimethylformamideHCID 6228—
Product1-(3-Chloropropyl)-1H-indoleHCID 2204896071%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 1-bromo-3-chloropropane (2.00 g, 12.7 mmol) in DMF (7.0 mL) was added indole (500 mg, 4.24 mmol) followed by powdered KOH (262 mg, 4.66 mmol) at 20° C. The reaction mixture was then stirred for 15 h at 20° C. The reaction was quenched by addition of H2O and the product was extracted with Et2O. The organic solution was washed with H2O and brine, dried over MgSO4, filtered and concentrated in vacuo. 1-(3-Chloro-1-propyl)indole (580 mg, 71%) was isolated by flash chromatography on a silica gel column by elution with EtOAc/Hexanes a pale yellow oil. 1H NMR (CDCl3, 300 MHz) δ2.28 (qu, 2H, J=6.3 Hz), 3.46 (t, 2H, J=6.2 Hz), 4.36 (t, 2H, J=6.6 Hz), 6.51 (d, 1H, J=3.3 Hz), 7.09-7.18 (m, 2H), 7.20-7.25 (m, 1H), 7.38 (d, 1H, J=8.5 Hz), 7.64 (d, 1H, J=7.7 Hz) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713471B1
Source datasetuspto-grants-2004_03
ORD IDord-fc1cbfbde0614814af42b2aeb590a66b
Source noteuspto-grants-2004_03