HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 13518986, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | alpha-Mercaptomethyl-beta-(p-nitrophenyl)-gamma-butyrolactone | HCID 20234198 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 13518986 | HCID 13518986 | 63.6% |
Reaction Steps
To a solution of 71 mg of potassium hydroxide in 6 ml of ethanol were added 253 mg of α-mercaptomethyl-β-(p-nitrophenyl)-γ-butyrolactone and 239 mg of benzyl bromide and the resulting mixture was kept at room temperature for 4 hours. After completion of the reaction, the reaction mixture was diluted with 60 ml of ethyl acetate, washed with water and saturated saline, dried over magnesium sulfate and the solvent was distilled off. The resulting crude product was purified by a silica gel column chromatography to give 218 mg (yield 50%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04613613 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-2cafb935f8da4155af7d1e7301adc72b |
| Source note | uspto-grants-1986_09 |