HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 178420436, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178527894 | HCID 178527894 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178420436 | HCID 178420436 | — |
Reaction Steps
A solution of 3-mercapto-1H-1,2,4-triazole (100 mg) and benzyl bromide (118 μl) in dimethylformamide (2 ml) was stirred at room temperature for 23 hours. To the reaction mixture were added ethyl acetate and saturated aqueous sodium hydrogencarbonate solution at room temperature, and the resultant mixture was extracted once with ethyl acetate. The organic layer was washed three times with water and subsequently once with saturated aqueous sodium chloride solution, and then dried over anhydrous sodium sulfate. The residue was filtered off, and the solvent was distilled from the resulting filtrate under reduced pressure to yield the titled compound (172 mg) as white solids.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238720B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-7ec5a70104fe4a99a340a8f2fbabe170 |
| Source note | uspto-grants-2007_07 |