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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567806Generated: November 1, 2026

tert-Butyl N-[3-(cyanomethyl)benzyl]-N-methylcarbamate → tert-Butyl N-[3-(2-aminoethyl)benzyl]-N-methylcarbamate

https://huagongshe.com/reaction/567806

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl N-[3-(cyanomethyl)benzyl]-N-methylcarbamateHCID 18470858—
CatalystNickelHCID 935—
SolventAmmoniaHCID 222—
SolventEthanolHCID 702—
Producttert-Butyl N-[3-(2-aminoethyl)benzyl]-N-methylcarbamateHCID 1847079578%

Reaction Steps

tert-Butyl-N-[3-(cyanomethyl)benzyl]-N-methylcarbamate (preparation 14) (3 g, 11.5 mmol, slightly impure) was dissolved in ethanol saturated with NH3 (300 ml), treated with Raney® Nickel (500 mg) and stirred under a hydrogen atmosphere (60 psi, room temperature, 18 hr). The catalyst was removed by filtration under nitrogen, the solvent evaporated to dryness and the resultant crude product purified by chromatography (SiO2, gradient elution with 100% CH2Cl2; 95:5 CH2Cl2:MeOH; 90:10 CH2Cl2:MeOH) to give the desired product (2.40 g, 78%). 1H NMR (CDCl3) δ 1.20 (s, 2H), 1.50 (s, 9H), 2.70-2.90 (m, 5H), 3.00 (s, 2H), 4.20 (s, br, 2H), 7.05 (s, br, 3H), 7.25 (s, br, 1H). LRMS m/z=265.1 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180627B2
Source datasetuspto-grants-2001_01
ORD IDord-20cb947ef3b7437f862d0e1e441f9ac8
Source noteuspto-grants-2001_01