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 | — |
Reaction Steps
To a solution of 3-hydroxyphenylacetic acid (Acros, 3.04 g, 20 mmol) in 20 mL of DMF were added K2CO3 (6.90 g, 50 mmol) and benzyl bromide (4.75 mL, 40 mmol) at room temperature. The reaction mixture was stirred for 24 h. The suspension was filtered and washed with diethyl ether. The filtrate was then washed with brine and dried over MgSO4. Filtration, followed by concentration, provided the crude benzyl 2-(3-(benzyloxy)phenyl)acetate which was used in the next step. MS (ESI+) m/z 355 (M+Na)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07459562B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-d1d7e62ef4c246a996af92dd24f83fd5 |
| Source note | uspto-grants-2008_12 |