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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337610Generated: October 30, 2026

Allyl bromide → 1-Allyl-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/337610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantIndole-3-CarboxaldehydeHCID 10256—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product1-Allyl-1H-indole-3-carbaldehydeHCID 801516—

Reaction Steps

Indole-3-carbaldehyde (1 eq.) was dissolved in DMF (0.46 M). Sodium hydride was added (2.5 eq.) and the resulting solution was stirred at RT for 20 min. Allyl bromide (1 eq.) was then added and the reaction solution was allowed to stir at RT for 20 h. The reaction mixture was subsequently quenched with brine and extracted with EtOAc. The combined organic extracts were dried over MgSO4. Filtration and concentration of the filtrate in vacuo afforded a yellow oil. Purification of the crude product thus obtained by way of flash chromatography (SiO2, 4:1 (v/v) Hex:EtOAc→3:7 (v/v) Hex:EtOAc) afforded the title compound as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-07bd0308512d4a52833cc5bbb00b9d0e
Source noteuspto-grants-2014_11