HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → o-Benzyloxyphenylacetic acid, benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2-Hydroxyphenyl)acetic acid | HCID 11970 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | o-Benzyloxyphenylacetic acid, benzyl ester | HCID 563142 | 96.7% |
Reaction Steps
To a solution of (2-hydroxyphenyl)acetic acid (125 g) in dimethylformamide (1.9 l) was added potassium carbonate (909 g) and benzyl bromide (281 g) successively. After being stirred for 18 hours, the mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate, washed with 1N aqueous sodium hydroxide solution and brine, dried and evaporated in vacuo. Dichloromethane was added to the residue and the solution was treated with activated carbon. The mixture was filtered and evaporated to give benzyl (2-benzyloxyphenyl)acetate (132 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06207686B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-3d17054a086d4b52b171d3986bd2ad16 |
| Source note | uspto-grants-2001_03 |