HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl fluoroacetate → Tert-butyl [1-(fluoroacetyl)piperidin-4-yl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl fluoroacetate | HCID 9988 | — |
| Reactant | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Solvent | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Product | Tert-butyl [1-(fluoroacetyl)piperidin-4-yl]carbamate | HCID 58959859 | 53.1% |
Reaction Steps
A solution of 500 mg of tert-butyl piperidin-4-ylcarbamate and 345 mg of ethyl fluoroacetate in 1 ml of trifluoroethanol was heated under reflux for 8 hours. The reaction mixture was concentrated under reduced pressure, and 1 M hydrochloric acid was added to the resulting residue. Then, this was extracted with EtOAc, and the organic layer was washed with aqueous saturated sodium hydrogencarbonate and brine. This was then dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The resulting residue was purified with silica gel column chromatography (eluent: chloroform to chloroform/methanol=30/1) to obtain 345 mg of tert-butyl [1-(fluoroacetyl)piperidin-4-yl]carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07268150B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-eb8c7975127e446cb5bbc0ccf744fa09 |
| Source note | uspto-grants-2007_09 |