HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 2-[5-(Ethoxycarbonyl)-2-oxo-1-azepanyl]butanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Ethyl 1-[1-(tert-butoxycarbonyl)propyl]-7-oxo-4-azepanecarboxylate | HCID 23545594 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[5-(Ethoxycarbonyl)-2-oxo-1-azepanyl]butanoic acid | HCID 21990303 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
In a 25 ml three necked flask fitted with magnetic stirrer and dropping funnel under inert atmosphere, 1 g (3.1 mmoles) of pure ethyl 1-[1-(tert-butoxycarbonyl)propyl]-7-oxo-4-azepanecarboxylate 29 was dissolved in 5 ml of CH2Cl2. The mixture was cooled down to 0° C., 5 ml of trifluoroacetic acid was added. The mixture was kept at 0° C. under stirring for 24 hours, concentrated to dryness and used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087596B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-645ca911aca9427b9ef5667e682c5d11 |
| Source note | uspto-grants-2006_08 |