HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 21469035, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 21469028 | HCID 21469028 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 21469035 | HCID 21469035 | 96.4% |
Reaction Steps
A mixture of 0.80 g of ethyl 4,5-dihydro-6-(4-nitrobenzoyl)-6H-thieno[3,2-d][1]-benzazepine-2-carboxylate in 25 ml of ethanol, 6 ml of tetrahydrofuran and 3.13 ml of 1M sodium hydroxide is stirred at room temperature for 22 hours. The mixture is acidified with 2 ml of 2M HCl and the solvents removed. The residue is dried under vacuum and extracted several times with CHCl3 --CH3 OH (1:1). The extracts are combined and the solvent removed to give 0.72 g of 4,5-dihydro-6-(4-nitro-benzoyl)-6H-thieno[3,2-d][1]benzazepine-2-carboxylic acid as a yellow solid; mass spectrum (CI) 395 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05693635 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-71b41fd444b440b9a75ffc9908856708 |
| Source note | uspto-grants-1997_12 |