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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74072Generated: October 25, 2026

Tert-butyl 2-tert-butyl-5-nitrobenzylcarbamate → Tert-butyl 2-tert-butyl-5-aminobenzylcarbamate

https://huagongshe.com/reaction/74072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-tert-butyl-5-nitrobenzylcarbamateHCID 57470261—
CatalystPalladiumHCID 23938—
SolventAcetic acid methanolHCID 10129899—
ProductTert-butyl 2-tert-butyl-5-aminobenzylcarbamateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829204B2
Source datasetuspto-grants-2014_09
ORD IDord-ece4a6dc8bde472d9adcd7d305ccd85b
Source noteuspto-grants-2014_09