HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 44278819, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19745915 | HCID 19745915 | — |
| Product | HCID 44278819 | HCID 44278819 | — |
Reaction Steps
At 0° C., 50% NaH in oil (37 mg) was added portionwise to a solution of 1-hydroxy-1-(4-2(-quinolinylmethoxy)phenyl)ethanol (Step 1) (104 mg) and benzyl bromide (92 mg). Stirring was continued for 18 h and the reaction was quenched with 25% aqueous NH4OAc. The product was extracted with EtOAc, dried over MgSO4 and purified by flash chromatography on silica gel using EtOAc:hexane (1:4) to give the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05102881 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-c8b777d5891841f38ad5f1b4dab512ff |
| Source note | uspto-grants-1992_04 |