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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840939Generated: October 29, 2026

Allyl bromide → HCID 23444834, compound

https://huagongshe.com/reaction/1840939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
ReactantHCID 23444865HCID 23444865—
SolventDimethylformamideHCID 6228—
ProductHCID 23444834HCID 23444834—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of 0.012 g (0.04 mmol) of a dispersion of 60% NaH in 0.5 mL of DMF, a solution of 0.042 g (0.01 mmol)of 2-(2-{4-[1-(2-hydroxy-ethyl)-1H-indol-3-yl]-piperidin-1-yl}-ethoxy)-benzoic acid in 0.5 mL of DMF was added. After stirring at room temperature for 30 minutes as solution of 0.014 g (0.12 mmol) of allyl bromide in 0.3 mL of DMF was added. The crude mixture was stirred at room temperature for 15 hours. The solvent was evaporated at reduced pressure and the crude mixture was dissolved in 1 mL of ethanol. 0.2 mL of an aqueous 2N NaOH solution were added and the mixture was heated at 60° C. for 3 hours. The solvent was removed under reduced pressure and after addition of 1 mL of water, the mixture was neutralised with 2N HCl and extracted with chloroform. The crude was purified by chromatography over silica gel affording 0.015 g (33% of yield) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683096B2
Source datasetuspto-grants-2004_01
ORD IDord-cf95811bb52f4b4d9642fd7f47e28972
Source noteuspto-grants-2004_01