HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 69334435, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Hydroxy-2-nitroestra-1,3,5(10)-trien-17-one | HCID 233496 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69334435 | HCID 69334435 | 99.1% |
Reaction Steps
To a solution of 3-hydroxy-2-nitroestra-1,3,5(10)-trien-17-one (76b, 1.58 g, 5.0 mmol) in DMF (20 mL) were added potassium carbonate (1.38 g, 10 mmol) and benzyl bromide (0.9 mL, 7.5 mmol) and stirred for 19 h at room temperature. To the reaction mixture was added saturated aqueous NH4Cl at 0° C. and extracted with CHCl3. The combined organic layers were washed with H2O, saturated aqueous NaCl, and then dried (Na2SO4). The desiccant was filtered and the solvent was evaporated at reduced pressure. The residue was washed with Et2O to afford 2.01 g of 79 (99% yield) mp: 234-235° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046186 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-6a13a30ca65b420c87bf8d45ddb81421 |
| Source note | uspto-grants-2000_04 |