HuagongsheHuagongshe Chemistry Print Report · For research reference only
hydroxylamine-O-sulfonic acid → Hexahydro-b-(4-methylphenyl)-2-oxo-1h-azepine-3-propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | hydroxylamine-O-sulfonic acid | HCID 76284 | — |
| Reactant | beta-(2-Oxocyclohexyl)-4-methylbenzenepropanoic acid | HCID 18800826 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | Hexahydro-b-(4-methylphenyl)-2-oxo-1h-azepine-3-propanoic acid | HCID 18800654 | — |
Reaction Steps
The title material of Example 201 in formic acid is added to a solution of hydroxylamine-O-sulfonic acid in formic acid over a 5 min. period with stirring under N2. The mixture is heated under reflux for 3 hours and then cooled to room temperature. The reaction is quenched with cold water and the solution is neutralized with 6N NaOH. It is then extracted three times with CH2Cl2. The combined organic layers are dried over MgSO4 and the solvent is removed on a rotary evaporator. The desired products are purified and isolated by HPLC to give both the 3- and 7-substituted title products.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06011028 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-b59c93c2adc946e8b3e24853d908d695 |
| Source note | uspto-grants-2000_01 |