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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981773Generated: October 30, 2026

1,6-Dibromohexane → 1-(6-Bromohexyl)-5-methoxy-2-(4-methoxyphenyl)-3-methyl-1H-indole

https://huagongshe.com/reaction/981773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,6-DibromohexaneHCID 12368—
ReactantSodium hydrideHCID 24758—
Reactant2-(4-METHOXYPHENYL)-3-METHYL-5-METHOXYINDOLEHCID 10880061—
SolventDimethylformamideHCID 6228—
Product1-(6-Bromohexyl)-5-methoxy-2-(4-methoxyphenyl)-3-methyl-1H-indoleHCID 1592563484%

Reaction Conditions

Temperature0 °C

Reaction Steps

12.5 mmol (300 mg) of NaH are added to 40 ml of absolute dimethylformamide and cooled to 0° C. With vigorous stirring, 7.5 mmol of 5-methoxy-2-(4-methoxy-phenyl)-3-methyl-indole dissolved in 25 ml of absolute dimethylformamide are slowly added dropwise and stirred for 30 minutes at 0° C. This suspension is added dropwise with stirring and ice-cooling to a solution of 11.0 mmol of 1,6-dibromohexane in 25 ml of absolute dimethylformamide and stirred for 30 minutes at 0° C. Excess NaH is destroyed with water and stirring continues for a further 2.5 hours at room temperature. The mixture is shaken with dichloromethane, dried over MgSO4 and the solvent removed. The brown oily crude product is chromatographed on silica gel with dichloro-methane and recrystallized from ethanol. Yield 84%. M.P. 60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04992553
Source datasetuspto-grants-1991_02
ORD IDord-f307a197ba904e618dca744910ca81de
Source noteuspto-grants-1991_02