HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → HCID 69669353, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 69669165 | HCID 69669165 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69669353 | HCID 69669353 | — |
Reaction Steps
Ammonium formate (1.2 g, 19.1 mmol) was added into a suspension of tert-butyl 4-(5-fluoro-2-nitrophenoxy)piperidine-1-carboxylate (2.0 g, 5.8 mmol) and palladium on carbon (5%, 0.4 g) in MeOH (30 mL) at ambient temperature. The solution was stirred for 0.5 hours, filtered through Celite and washed with MeOH. The filtrate was concentrated in vacuo and triturated from diethyl ether to remove the ammonium formate by-products. The sample was purified by flash column chromatography (1:10→1:1 EtOAc/DCM) to yield a colourless oil which crystallised from diethyl ether/petroleum ether (40-60° C.) as a colourless solid (1.6 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486953B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-e9a730ca4f7340dfba5b660736f37004 |
| Source note | uspto-grants-2013_07 |