HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Ethyl 2-(3-(benzyloxy)phenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl (3-Hydroxyphenyl)acetate | HCID 572437 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-(3-(benzyloxy)phenyl)acetate | HCID 15197900 | — |
Reaction Steps
To a stirred solution of Ethyl 2-(3-hydroxyphenyl)acetate (3 g, 16.6 mmol) in DMF (25 ml) was added potassium carbonate (2.99 g, 21.6 mmol) at room temperature followed by drop wise addition of benzyl bromide (3.13 g, 18.3 mmol). The reaction mixture was stirred for 16 hours and taken in ethyl acetate, washed with water (2×) and brine. The organic layer was dried over Na2SO4, filtered, concentrated and purified by flash chromatography on a silica gel column (hex:ethyl acetate 4:1) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829058B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-2fa8b255ea42414390f3be2390c361f0 |
| Source note | uspto-grants-2014_09 |