HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → Ethyl 5-acetyl-4-hydroxy-3-methylbenzofuran-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Ethyl 4-hydroxy-3-methyl-1-benzofuran-2-carboxylate | HCID 748649 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | Ethyl 5-acetyl-4-hydroxy-3-methylbenzofuran-2-carboxylate | HCID 20205101 | 59% |
Reaction Steps
To 4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester 0.5 g (2.27 mmol) was added 15 mL of chlorobenzene, 0.27 g (3.4 mmol) of acetyl chloride and 0.63 mL (5.7 mmol) of titanium tetrachloride. The mixture was sealed in a pressure tube and the tube was placed in 95° C. oil bath for 5 h with stirring. The reaction mixture was washed with 0.5N HCl and was extracted with ethyl acetate. Removal of the solvents gave the crude product, which was purified by column chromatography to give 0.33 g (59% yield) of 5-acetyl-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07420001B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-2be44430397b41dab8f07180b2815339 |
| Source note | uspto-grants-2008_09 |