HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → (3-Benzyloxyphenyl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3'-Hydroxyphenylacetic acid | HCID 12122 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Benzyloxyphenyl)acetic acid | HCID 4592030 | 91% |
Reaction Steps
A mixture of 2-(3-hydroxyphenyl)acetic acid (0.6 g, 3.95 mmol), benzyl bromide (0.710 g, 4.14 mmol), potassium hydroxide (0.550 g, 9.87 mmol), KI (13 mg, 0.079 mmol) in THF (20 mL) was refluxed for 18 h. The solvent was removed and the residue was dissolved in 50 mL of water and extracted with ether. The aqueous layer was acidified with aqueous 1N HCl and the white precipitate that formed was filtered off to afford 2-(3-(benzyloxy)phenyl)acetic acid as a gray solid (0.87 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09126993B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-5a7a5848dd824c23aabd1d22ff5b346b |
| Source note | uspto-grants-2015_09 |