HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 89739301, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13138782 | HCID 13138782 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 89739301 | HCID 89739301 | 46.2% |
Reaction Steps
To a solution of 21 (0.5 mg, 1.8 mmol) in acetonitrile (3 mL) was added sodium hydride (0.11 g, 2.7 mmol) at 0° C. A solution of benzyl bromide (0.48 mL, 2 mmol) in acetonitrile (2 mL) was then added to the mixture dropwise, under an argon atmosphere. The reaction was stirred for 16 h at room temperature. Upon completion, distilled water (10 mL) was added to the mixture and the organic layer extracted into ethyl acetate. The organic layers were combined, dried and concentrated to give a crude mixture that was purified by column chromatography (Silica gel, 10%-20% EtOAc in hexane) to give 22 (300 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09422320B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-060fb05cb6794d4aa06b1f4c17a8d00e |
| Source note | uspto-grants-2016_08 |