HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Methyl benzofuran-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 20043642 | HCID 20043642 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl benzofuran-7-carboxylate | HCID 14229730 | 25.2% |
Reaction Steps
A mixture of 2.09 g of (2-methoxycarbonyl-6-formylphenoxy)acetic acid, 1.48 g of sodium acetate and 7 ml of acetic anhydride is refluxed for 1.5 hours. After cooling, water is added to the reaction mixture, and the aqueous mixture is alkalized with potassium carbonate and extracted with ethyl acetate. The extract is washed with water, dried and evaporated to remove solvent. The residue is purified by silica gel column chromatography to give 0.39 g of methyl benzofuran-7-carboxylate as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04829067 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-26d14820452b407593991de30db3ffae |
| Source note | uspto-grants-1989_05 |