HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(Tert-butoxycarbonylamino-methyl)-2-nitro-benzoic acid → 2-Amino-5-({[(tert-butoxy)carbonyl]amino}methyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(Tert-butoxycarbonylamino-methyl)-2-nitro-benzoic acid | HCID 66697149 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Amino-5-({[(tert-butoxy)carbonyl]amino}methyl)benzoic acid | HCID 66697138 | 49.3% |
Reaction Steps
A mixture of 5-(tert-butoxycarbonylamino-methyl)-2-nitro-benzoic acid (21.0 g, 70.9 mmol) in methanol (210 mL) and palladium/carbon (2 g) was hydrogenated with a Parr-shaker overnight at 51 psi. The black mixture was filtered through a pad of Celite, and the filtrate was evaporated to give a brown oil, which was stirred in ether (300 mL) overnight. The ether slurry was filtered to give 2-amino-5-(tert-butoxycarbonylamino-methyl)-benzoic acid as a brown solid (9.3 g, 49% yield). The product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492395B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-828118460ea14332a26c0874f5335e8d |
| Source note | uspto-grants-2013_07 |