HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 14820506, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzo[b]thiophene-5-ol, 2,3-dihydro- | HCID 11367101 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 14820506 | HCID 14820506 | 83.4% |
Reaction Steps
To a solution of 5-hydroxy-2,3-dihydrobenzothiophene (1.53 g, 10.05 mmoles) in 200 mL acetone was added K2CO3 (12.5 g, 90.45 mmoles) with good mechanical stirring. The suspension was warmed and allyl bromide (4.86 g, 40.20 mmoles) was added in one portion. The reaction mixture was then heated to reflux overnight. After cooling, the solids were removed by filtration and the filtrate concentrated. The residue was taken up in 50/50 vol/vol hexane/methylene chloride and refiltered to remove the remaining salts. Concentration afforded 3.2 q crude product (a yellow oil) which was purified by flash chromatography (3% EtOAc in hexane to elute) to give 1.61 g pure product (83.4%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04963580 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-f0097dec01dd4648a6d02265a4057a28 |
| Source note | uspto-grants-1990_10 |