HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-(2-Pyrrolidin-1-ylethoxy)benzofuran-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 5-(2-Pyrrolidin-1-ylethoxy)benzofuran-2-carboxylic acid methyl ester | HCID 66688208 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(2-Pyrrolidin-1-ylethoxy)benzofuran-2-carboxylic acid | HCID 22928319 | 58.1% |
Reaction Steps
To an ice-cooled solution of 5-(2-pyrrolidin-1-ylethoxy)benzofuran-2-carboxylic acid methyl ester (960 mg, 3.3 mmol) anhydrous ethylene glycol dimethyl ether (10 ml) was added dropwise degassed aqueous lithium hydroxide solution (2.0 ml, 2.0M). After stirring at room temperature for 4 h, the solution was cooled down and the pH was adjusted to 2 with 4.0 M HCl in dioxane. A gummy tan precipitate formed. The solvent was removed and the gummy residue was frozen and lyophilized. The tan colored solid was dissolved in boiling 2-propanol (90 ml), the solution was filtered hot and then cooled to give 5-(2-pyrrolidin-1-yl-ethoxy)-benzofuran-2-carboxylic acid as beige colored needles (528 mg). Additional 153 mg was obtained from the mother liquor.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07834054B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-91effea2306a48d79f15731f4d9ceef7 |
| Source note | uspto-grants-2010_11 |