HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Carboxy-4-methoxy-3-(2-phenylethyl)benzo[b]thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Methoxy-2-methoxycarbonyl-3-(2-phenylethyl)benzo[b]thiophene | HCID 23103548 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Carboxy-4-methoxy-3-(2-phenylethyl)benzo[b]thiophene | HCID 23103520 | 95.9% |
Reaction Steps
To a solution of 4-methoxy-2-methoxycarbonyl-3-(2-phenylethyl)benzo[b]thiophene (1.09 g) in tetrahydrofuran (6 mL)-methanol (21 mL) was added 1 mol/L aqueous sodium hydroxide solution (21 mL), and the mixture was heated for reflux for 3.5 hours. The reaction mixture was cooled to room temperature. To the mixture was added 2 mol/L hydrochloric acid (11 mL), and the precipitated crystals were collected by filtration. The crystals were dried under reduced pressure to give the title compound (1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07566699B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-577da371a756430ebeb9460efc8effec |
| Source note | uspto-grants-2009_07 |