HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Benzyl 2-(3-(benzyloxy)phenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3'-Hydroxyphenylacetic acid | HCID 12122 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl 2-(3-(benzyloxy)phenyl)acetate | HCID 15470856 | 198.6% |
Reaction Steps
To a solution of 3-hydroxyphenyl acetic acid (5.0 g, 0.03 mol) in DMF (25 ml) was added potassium carbonate (12.4 g, 0.09 mol). The reaction was allowed to stir for twenty minutes at which time benzyl bromide (8.9 ml, 0.075 mol) was added to the flask. The reaction was allowed to stir overnight. Solvent was removed. The reaction was diluted with water and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated to yield the title compound (9.9 g, 99% yield): ES-MS (m/z) 243 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07435729B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-bae80bde2a3848909adaef6ca36c8524 |
| Source note | uspto-grants-2008_10 |