HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → 2-[(Prop-2-yn-1-yl)sulfanyl]-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Indolinethione | HCID 3032310 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-[(Prop-2-yn-1-yl)sulfanyl]-1H-indole | HCID 20284771 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04256640 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-6ef44c71cfa8464f8e6d519c2943171b |
| Source note | uspto-grants-1981_03 |