HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 2-tert-butyl-5-nitrobenzylcarbamate → Tert-butyl 2-tert-butyl-5-aminobenzylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 2-tert-butyl-5-nitrobenzylcarbamate | HCID 57470261 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic acid methanol | HCID 10129899 | — |
| Product | Tert-butyl 2-tert-butyl-5-aminobenzylcarbamate | HCID 57470262 | — |
Reaction Steps
To a solution of tert-butyl 2-tert-butyl-5-nitrobenzylcarbamate (20 mg, 0.065 mmol) in 5% AcOH-MeOH (1 mL) was added 10% Pd—C (14 mg) under nitrogen atmosphere. The mixture was stirred under H2 (1 atm) at room temperature for 1 h. The catalyst was removed via filtration through Celite, and the filtrate was concentrated to give tert-butyl 2-tert-butyl-5-aminobenzylcarbamate (E-4), which was used without further purification. 1H NMR (400 MHz, CDCl3) δ 7.09 (d, J=8.5 Hz, 1H), 6.62 (d, J=2.6 Hz, 1H), 6.47 (dd, J=8.5, 2.6 Hz, 1H), 4.61 (br s, 1H), 4.40 (d, J=5.1 Hz, 2H), 4.15 (br s, 2H), 1.39 (s, 9H), 1.29 (s, 9H); HPLC ret. time 2.47 min, 10-100% CH3CN, 5 min gradient; ESI-MS 279.3 m/z (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829204B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-ece4a6dc8bde472d9adcd7d305ccd85b |
| Source note | uspto-grants-2014_09 |