HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 131729222, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 53913110 | HCID 53913110 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131729222 | HCID 131729222 | — |
Reaction Steps
A solution of 2.62 g of the compound obtained in Step 86-1 in DMF (30 ml) was added sequentially 1.29 g of K2CO3 and benzyl bromide (1.1 ml), and the reaction mixture was stirred at room temperature for 3 hours. The solution was cooled on ice, then, a saturated aqueous solution of NaHCO3 was added, and the mixture was extracted with EtOAc. The combined organic layer was washed with water and saturated brine, dried over MgSO4, then, the drying agent was separated by filtration and the solvent was evaporated under reduced pressure. The obtained residue was purified by column chromatography (silicagel 60; mobile phase: n-hexane/EtOAc=1/1; v/v) to obtain 2.36 g of the title compound (colorless oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030499B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-72b27cf11ca8485bbb60221b6393cc6f |
| Source note | uspto-grants-2011_10 |