HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 2-(4-fluoro-3-nitrobenzamido)acetate → 2-(3-Amino-4-fluorobenzamido)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 2-(4-fluoro-3-nitrobenzamido)acetate | HCID 86713118 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(3-Amino-4-fluorobenzamido)acetic acid | HCID 73437830 | 70% |
Reaction Steps
To a solution of benzyl 2-(4-fluoro-3-nitrobenzamido)acetate (85 mg) in EtOAc (10 mL) was added Pd/C (10%, 100 mg) at rt and stirred under the atmosphere of H2 gas for 25 min. Work-up of the reaction mixture as described in example 1 gave the product as a white color solid (38 mg, 70%), mp 150-152° C. 1H NMR (400 MHz, CDCl3+DMSO-d6): δ 7.74 (1H, br s), 7.37 (1H, dd, J=8.6, 1.8 Hz), 7.12-7.16 (1H, m), 6.97 (1H, dd, J=10.6, 8.6 Hz), 4.07 (2H, d, J=5.6 Hz); 13C NMR (100 MHz, CDCl3+DMSO-d6): δ 170.6, 165.9, 151. 9 (d, J=242 Hz), 134.5 (d, J=13 Hz), 129.6 (d, J=3 Hz), 115.4 (d, J=8 Hz), 115.1 (d, J=6 Hz), 113.6 (d, J=19 Hz), 40.5; LC-MS (negative ion mode): m/z 211 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08906344B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-0c95adb23b0343bda67f1ae9c4c371b0 |
| Source note | uspto-grants-2014_12 |