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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821960Generated: October 31, 2026

1-Bromoheptane → 5-Benzyloxy-1-heptylindole

https://huagongshe.com/reaction/1821960

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromoheptaneHCID 12369—
Reactant5-BenzyloxyindoleHCID 14624—
ReactantPotassium HydroxideHCID 14797—
CatalystTetrabutylammonium BromideHCID 74236—
Product5-Benzyloxy-1-heptylindoleHCID 68842666—

Reaction Steps

0.22 g (4.45 mmol) pulverized, 88% potassium hydroxide, 0.5 g (2.24 mmol) 5-benzyloxyindole and 0.07 g (0.22 mmol) tetrabutylammoniumbromide are weighed out in the given order and mixed with 1.41 ml (8.96 mmol) 1-bromoheptane with vigorous stirring. The mixture is stirred at room temperature overnight. Having added 30 ml water, three extractions using diethyl ether are carried out. The organic phase is washed three times with saturated NaCl solution, dried on sodium sulfate and the solvent is removed in vacuo. The residue is purified on silica gel by means of column chromatography (flow agent: hexane/ethyl acetate 95:5). The product accrues as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608633B2
Source datasetuspto-grants-2009_10
ORD IDord-149482f5fe0e4210882e07c51aa50255
Source noteuspto-grants-2009_10