HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 13397856, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isothiazolo(5,4-b)pyridin-3(2H)-one, 4,6-dimethyl- | HCID 173760 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13397856 | HCID 13397856 | — |
Reaction Steps
Triethylamine (approximately 3 ml) is added to a slurry of 5.0 g of 4,6-dimethylisothiazolo-(5,4-b)-pyridin-3(2H)-one in 120 ml reagent grade acetone until the mixture becomes homogeneous. A solution of 4.0 g (0.024 m) of benzyl bromide in 20 ml acetone is then added. The reaction mixture is stirred for 3 days at room temperature and is then stripped to dryness. The residue is washed once with deionized water, then with 95% 2B ethanol, then ether and dried to give the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03965107 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-bd9889eed4f0420ba8ab015478bf896e |
| Source note | uspto-grants-1976_06 |