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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430777Generated: November 2, 2026

(3-Bromopropyl)benzene → HCID 18351837, compound

https://huagongshe.com/reaction/430777

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Bromopropyl)benzeneHCID 12503—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 18351819HCID 18351819—
SolventDimethylformamideHCID 6228—
ProductHCID 18351837HCID 1835183796%

Reaction Steps

Under argon atmosphere, sodium hydride (40 mg) was added to 1-(2-hydroxyethyl)-4-benzyloxyindole (52 mg) in DMF (3 ml) and the mixture was stirred at room temperature for 15 minutes. To the mixture, 3-phenyl-1-bromopropane (0.15 ml) was added and the resultant was stirred at room temperature for another 18 hours. The reaction mixture was added to saturated aqueous NH4Cl solution (5 ml) to stop the reaction, and the resultant was extracted with ethyl acetate (3×10 ml). The obtained organic layers were washed with saturated brine and dried over sodium sulfate. After removing solids by filtration, the solvent was removed under reduced pressure, and the obtained crude product was purified by silica gel column chromatography to obtain the desired compound (72 mg, yield: 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323235B1
Source datasetuspto-grants-2001_11
ORD IDord-b3229e56cac24aabac1809125493d01e
Source noteuspto-grants-2001_11