HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Benzoic acid, 5-acetyl-2-(phenylmethoxy)-, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 5-acetylsalicylate | HCID 85444 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | Benzoic acid, 5-acetyl-2-(phenylmethoxy)-, methyl ester | HCID 12368981 | 71.4% |
Reaction Steps
A mixture of 5-acetylsalicylic acid methyl ester (13.59 g, 70 mmol), benzyl bromide (17.96 g, 105 mmol), potassium carbonate (19.35 g, 140 mmol) and methyl ethyl ketone (350 mL) was refluxed for 8 hours. After cooling, the solvent was evaporated under reduced pressure. 2N Hydrochloric acid was added to the residue, and it was extracted with ethyl acetate. After the ethyl acetate layer was washed with water and brine, dried over anhydrous magnesium sulfate and concentrated, the residue was recrystallized from isopropyl ether to give the title compound (14.20 g, 71.4%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700655B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-189be7c814b34ef484c25ee1d7da93da |
| Source note | uspto-grants-2010_04 |