HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid ethanol → ethyl (2E)-4-aminobut-2-enoate trifluoroacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid ethanol | HCID 19378329 | — |
| Reactant | ethyl (2E)-4-(diformylamino)but-2-enoate | HCID 58465259 | — |
| Product | ethyl (2E)-4-aminobut-2-enoate trifluoroacetate | HCID 72699081 | — |
Reaction Steps
A solution of ethyl (2E)-4-(diformylamino)but-2-enoate (XV) (0.89 mg, 4.8 mmol) in a mixture trifluoroacetic acid-ethanol (absolute) (2:1, 10 mL) was stirred under reflux overnight (the reaction was followed by LC-MS and stopped when complete conversion was achieved). The solvent was evaporated under vacuum to obtain compound ethyl (2E)-4-aminobut-2-enoate trifluoroacetate (IV) as brown oil (undetermined yield), which was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08394802B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-c53ed8279bff4145b331eca797379488 |
| Source note | uspto-grants-2013_03 |