HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 12827154, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Cyclohexene-1,4-diol | HCID 550825 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12827154 | HCID 12827154 | — |
Reaction Steps
To a solution of 34 (79 mg, 0.69 mmol) in DMF (1 mL) was added sodium hydride (14 mg, 0.62 mmol) at 0° C. Benzyl bromide (73 μL, 0.62 mmol) was added to the mixture dropwise, under an argon atmosphere. The reaction was stirred for 16 h at room temperature. Upon completion, distilled water (3 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 35 as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09422320B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-ec927e1369724cf0bc30af60a8959100 |
| Source note | uspto-grants-2016_08 |