HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → [2-(5-chlorothiophen-2-yl)-1H-benzimidazol-5-yl]acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178470643 | HCID 178470643 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [2-(5-chlorothiophen-2-yl)-1H-benzimidazol-5-yl]acetic acid | HCID 178525013 | — |
Reaction Steps
3.2 34.7 ml of aqueous 1 N sodium hydroxide solution are added to a solution of 10.1 g (about 20.5 mmol) of ethyl [2-(5-chlorothiophen-2-yl)-1H-benzimidazol-5-yl]acetate in 70 ml of methanol, and the mixture is stirred at room temperature for 3 days. The reaction mixture is evaporated, and the residue is taken up in 25 ml of water. A pH of 4.5 is set by addition of conc. hydrochloric acid. The resultant precipitate is filtered off, washed with water and dried, giving [2-(5-chlorothiophen-2-yl)-1H-benzimidazol-5-yl]acetic acid as a yellowish solid; ESI 293.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07566789B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-7b69e652f31845f9ba00889a84ca3bca |
| Source note | uspto-grants-2009_07 |