Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127508Generated: November 3, 2026

Propargyl bromide → 2-[(Prop-2-yn-1-yl)sulfanyl]-1H-indole

https://huagongshe.com/reaction/127508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
Reactant2-IndolinethioneHCID 3032310—
SolventAcetoneHCID 180—
Product2-[(Prop-2-yn-1-yl)sulfanyl]-1H-indoleHCID 2028477198%

Reaction Steps

To a solution of the product (14.9 g) of the above (1) in acetone (250 ml) are added potassium carbonate (16.5 g) and propargyl bromide (14.3 g) successively and the mixture is stirred at room temperature for three hours. The precipitate is filtered off. The filtrate is condensed and extracted with ether after addition of water. The extract is washed with water, dried and evaporated to remove the solvent yielding an oily residue (23 g). The residue is chromatographed on a column of silica gel (100 g) and eluted with benzene-hexane. The eluate is condensed to give the tile compound as an oil (18.3 g). Yield: 98%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256640
Source datasetuspto-grants-1981_03
ORD IDord-6ef44c71cfa8464f8e6d519c2943171b
Source noteuspto-grants-1981_03