HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetovanillone → Ethyl (4-acetyl-2-methoxyphenoxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetovanillone | HCID 2214 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl (4-acetyl-2-methoxyphenoxy)acetate | HCID 23282600 | — |
Reaction Steps
To dimethylformamide (200 ml) are added 2-methoxy-4-acetylphenol (20 g), ethyl α-bromoacetate (15 ml) and potassium carbonate (18.3 g), and the mixture is stirred at room temperature overnight. After the reaction is complete, water is added to the mixture, and the mixture is extracted with ethyl acetate. The extract is washed with aqueous sodium hydrogen carbonate solution, and dried over magnesium sulfate, and concentrated under reduced pressure to remove the solvent. The resulting crystals are collected, and washed with n-hexane-diethyl ether to give ethyl α-(2-methoxy-4-acetylphenoxy)acetate (23.86 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06140330 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-19a46f397f50424093ccc89a1b6dd616 |
| Source note | uspto-grants-2000_10 |