HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Tert-butyl-3-nitro-phenyl)-carbamic acid tert-butyl ester → (3-Amino-4-tert-butyl-phenyl)-carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Tert-butyl-3-nitro-phenyl)-carbamic acid tert-butyl ester | HCID 66675534 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (3-Amino-4-tert-butyl-phenyl)-carbamic acid tert-butyl ester | HCID 51358180 | 93% |
Reaction Steps
A suspension of (4-tert-butyl-3-nitro-phenyl)-carbamic acid tert-butyl ester (3.0 g, 10.19 mol) and 10% Pd—C (1 g) in MeOH (40 mL) was stirred under H2 (1 atm) at room temperature overnight. After filtration, the filtrate was concentrated and the residue was purified by column chromatograph (petroleum ether-EtOAc, 5:1) to give (3-amino-4-tert-butyl-phenyl)-carbamic acid tert-butyl ester (D-10) as a brown oil (2.5 g, 93%). 1H NMR (CDCl3) δ 7.10 (d, J=8.4 Hz, 1H), 6.92 (s, 1H), 6.50-6.53 (m, 1H), 6.36 (s, 1H), 3.62 (br s, 2H), 1.50 (s, 9H), 1.38 (s, 9H); ESI-MS 528.9 m/z (2M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08324242B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-891dcfb56fdf45d4ba6d6e36ef4dd2bb |
| Source note | uspto-grants-2012_12 |