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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423913Generated: October 29, 2026

Ammonium formate → Tert-Butyl (2-(4-aminophenyl)-2-methylpropyl)carbamate

https://huagongshe.com/reaction/423913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantTert-butyl 2-methyl-2-(4-nitrophenyl)propylcarbamateHCID 22981239—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductTert-Butyl (2-(4-aminophenyl)-2-methylpropyl)carbamateHCID 2298116783.2%

Reaction Steps

To a refluxing solution of tert-butyl 2-methyl-2-(4-nitrophenyl)propylcarbamate (725 mg, 2.5 mmol) and ammonium formate (700 mg, 10.9 mmol) in EtOH (25 mL) was added Pd-5% wt on carbon (400 mg). The mixture was refluxed for 1 h, cooled and filtered through Celite. The filtrate was concentrated to give tert-butyl 2-methyl-2-(4-aminophenyl)propylcarbamate (G-3) (550 mg, 83%), which was used without further purification. 1H NMR (400 MHz, DMSO-d6) δ 6.99 (d, J=8.5 Hz, 2H), 6.49 (d, J=8.6 Hz, 2H), 4.85 (s, 2H), 3.01 (d, J=6.3 Hz, 2H), 1.36 (s, 9H), 1.12 (s, 6H); HPLC ret. time 2.02 min, 10-99% CH3CN, 5 min run; ESI-MS 265.2 m/z (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101767B2
Source datasetuspto-grants-2012_01
ORD IDord-1d55a7f4fc9942a8836c1ef6d6dca8e4
Source noteuspto-grants-2012_01