HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 18655844, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 54043047 | HCID 54043047 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18655844 | HCID 18655844 | — |
Reaction Steps
trans-2-(3-Methoxy-4-propoxy-5-aminophenyl)-5-(3,4,5-trimethoxyphenyl)-tetrahydrothiophene (10 mg, 0.023 mmole) and potassium carbonate (0.2 g) were suspended in 1 mL DMF. To this mixture was added benzyl bromide (39.50 mg, 0.23 mmole). The mixture was stirred at room temperature for 20 hours, quenched with water, and then extracted with dichloromethane. The organic layer was dried over MgSO4, filtered and evaporated in vacuo to an oil that was purified by column chromatography using hexane/ethyl acetate (3:1) as solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05856323 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-e8eb136655144bc7b5744c3d3dcbdc2b |
| Source note | uspto-grants-1999_01 |