HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 66750789, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 66750740 | HCID 66750740 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66750789 | HCID 66750789 | — |
Reaction Steps
A mixture of 5-(3-benzyloxy-6-hydroxy-5,6,7,8-tetrahydronaphthalen-2-yl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one (90 mg, 0.23 mmol) from preparing Example 45, benzyl bromide (0.033 mL, 0.28 mmol) and potassium carbonate (63 mg, 0.46 mmol) in DMF (2 mL) is stirred at RT for 18 h. The mixture is partitioned between EtOAc and 1 N HCl solution. The organic extract is dried with MgSO4 and concentrated. The residue is purified to give the title compound as an oil: (M+NH4)+=478.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700633B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-3180e8833953433f91bcd75c0e9fb485 |
| Source note | uspto-grants-2010_04 |