HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3-(benzyloxy)-2-thiophenecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | methyl 3-(benzyloxy)-2-thiophenecarboxylate | HCID 2764114 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(benzyloxy)-2-thiophenecarboxylic acid | HCID 2766733 | 91.3% |
Reaction Steps
To a solution of methyl 3-(benzyloxy)-2-thiophenecarboxylate (7.85 g, 31.61 mmol) in MeOH (32 mL) and THF (16 mL) was added 2 N NaOH (21 mL), and the mixture was stirred at reflux for 10 hrs, and then concentrated under reduced pressure. The residue was diluted with water, washed with ether. The separated aqueous phase was acidified with 5N HCl. The precipitated solid was collected by filtration, washed with hexane, and dried under reduced pressure at 60° C. to give 3-(benzyloxy)-2-thiophenecarboxylic acid as a yellow solid (6.76 g, yield; 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562811B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-d8052d36ca3b42e9b280de495f70cb7d |
| Source note | uspto-grants-2003_05 |