HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Benzyl 3-(4-benzyloxyphenyl)propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3-(4-Hydroxyphenyl)propionic acid | HCID 10394 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl 3-(4-benzyloxyphenyl)propionate | HCID 14281237 | 89.3% |
Reaction Steps
3-(4-Hydroxyphenyl)propionic acid (5 g), potassium carbonate (16 g) and tetrahydrofuran (50 ml) were placed in a three-necked flask, 8.5 ml of benzyl bromide was added dropwise through a syringe under stirring, and the mixture was heated under reflux overnight. After filtering off the solid matters, the solvent was distilled off, and the residue was purified by column chromatography on silica gel (50 g), affording 9.25 g (89.3%) of pure benzyl 3-(4-benzyloxyphenyl)propionate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04775743 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-8f6f6c880386459ea0522d24ad9b32f8 |
| Source note | uspto-grants-1988_10 |