HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 67109597, compound → HCID 67109671, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 67109597 | HCID 67109597 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67109671 | HCID 67109671 | 101.3% |
Reaction Steps
A solution of tert-butyl 2-(benzyloxy)-4-fluorobenzylcarbamate (Example 14; 9 mmol) in EtOH (80 ml) and ethyl acetate (240 ml) was treated with 1 atm of hydrogen at 25° C. over 10% Pd/C (0.4 gr) for 24 hours. The catalyst was removed by filtration through celite, washed with EtOH and the filtrate was concentrated to afford the title compound (2.2 g) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08497270B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-56b64e6ec5e74b188e5eddf5ffc60d44 |
| Source note | uspto-grants-2013_07 |