HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 7-((2-((Tert-butoxycarbonyl)amino)phenyl)amino)-7-oxoheptanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 7-((2-((tert-butoxycarbonyl)amino)phenyl)amino)-7-oxoheptanoate | HCID 90388837 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-((2-((Tert-butoxycarbonyl)amino)phenyl)amino)-7-oxoheptanoic acid | HCID 9543538 | 92.6% |
Reaction Steps
To a solution of Ethyl 7-((2-((tert-butoxycarbonyl)amino)phenyl)amino)-7-oxoheptanoate (14 g, 37 mmol) in Ethanol (80 mL) was added KOH (6.2 g, 111 mmol) and water (80 mL). The mixture was stirred at room temperature for 4 hours, and then concentrated under reduce pressure. The pH value of the solution was adjusted to 4 by concentrated HCl. The resulting mixture was extracted by EtOAc (200 mL×3). The organic layers were combined and dried over Na2SO4, then concentrated to give the desired compound (12 g, yield 92.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133105B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-0549be732c5441a18a132d728a19f116 |
| Source note | uspto-grants-2015_09 |