HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-Ethoxycarbonylmethoxy-3-methyl-benzofuran-2-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 4-Hydroxy-3-methyl-benzofuran-2-carboxylic acid tert-butyl ester | HCID 13849456 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Ethoxycarbonylmethoxy-3-methyl-benzofuran-2-carboxylic acid tert-butyl ester | HCID 68714959 | 90% |
Reaction Steps
To a round bottom flask with a stir bar was added 4-hydroxy-3-methyl-benzofuran-2 carboxylic acid t-butyl ester (1 mmol), ethyl 2-bromoacetate (1.1 eq.) potassium carbonate (5 equiv.), and 10 mL of DMF. The reaction mixture was stirred overnight and then slowly added dropwise to water (10 mL) with stirring. The resulting mixture was extracted with ethyl acetate (2×20 mL), brine (20 mL), dried over magenesium sulfate. Filtration and evaporation of the solvent gave 4-ethoxycarbonylmethoxy-3-methyl-benzofuran-2-carboxylic acid tert-butyl ester as a thick oil in 90% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07420001B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-950dceff36ee4758b28dfce462a94429 |
| Source note | uspto-grants-2008_09 |