HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 7-(4-Morpholinophenyl)-2,3-dihydro-1-benzothiepine-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 7-(4-morpholinophenyl)-2,3-dihydro-1-benzothiepine-4-carboxylate | HCID 18472523 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | 7-(4-Morpholinophenyl)-2,3-dihydro-1-benzothiepine-4-carboxylic acid | HCID 18472275 | 94.8% |
Reaction Steps
To a solution of methyl 7-(4-morpholinophenyl)-2,3-dihydro-1-benzothiepine-4-carboxylate (0.55 g) in ethanol/THF (30/30 ml) was added at room temperature 1N sodium hydroxide solution (1.8 ml), and the mixture was stirred for 6 days and then refluxed for 2 hours. To the mixture was added 1N hydrochloric acid (1.8 ml). The resulting solid was collected by filtration, which was washed with ethanol and diethylether to give yellow powder of 7-(4-morpholinophenyl)-2,3-dihydro-1-benzo-thiepine-4-carboxylic acid (502.2 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172061B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-eb40cbd0441b4fe5bc7713156119c134 |
| Source note | uspto-grants-2001_01 |