HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 501233, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178516238 | HCID 178516238 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 501233 | HCID 501233 | 65.7% |
Reaction Steps
To a mixture of 10.0 g of 2-mercapto-3-pyridinol, 11.0 g of potassium carbonate and 100 mL of 2-butanone was added dropwise with stirring, 13.3 g of benzyl bromide. After stirring at 22° C. for two hours, the mixture was heated to reflux for thirty minutes. The reaction mixture was concentrated under reduced pressure, the residue treated with water, and the mixture brought to pH 6 by the addition of acetic acid. The crude product was filtered and recrystallized from toluene to give 11.1 g of the title compound as a grey crystalline solid, mp 103–104° C. The structure of the product was confirmed by its 1H nmr and mass spectra.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07064139B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-997956b4e4d94a9bb1e879853d7bf065 |
| Source note | uspto-grants-2006_06 |