HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 3-(2-Oxo-2-(piperazin-1-yl)ethoxy)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-Butyl 4-(2-(3-formylphenoxy)acetyl)piperazine-1-carboxylate | HCID 89725867 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2-Oxo-2-(piperazin-1-yl)ethoxy)benzaldehyde | HCID 89726202 | — |
Reaction Steps
tert-butyl 4-(2-(3-formylphenoxy)acetyl)piperazine-1-carboxylate (49)/(5.55 mmol) was taken in DCM and cooled to 0° C. when TFA (5 ml) was added drop wise and then stirred at rt for 16 h when TLC confirmed completion of reaction. The reaction mixture was concentrated and neutralized with satd NaHCO3 solution followed by extraction with DCM. The combined organic extracts was dried, concentrated and used directly for the next step (86%). LCMS: 98.12% (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238656B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-c18d9be70abe4cc89c3413b3ee5ddc00 |
| Source note | uspto-grants-2016_01 |