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HRID 2238447Erstellt: 25. Oktober 2026

Benzyl 2-(di-tert-butoxyphosphoryloxy)ethylcarbamate → 2-Aminoethyl di(tert-butyl) phosphate

https://huagongshe.com/reaction/2238447

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl 2-(di-tert-butoxyphosphoryloxy)ethylcarbamateHCID 68635482—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt2-Aminoethyl di(tert-butyl) phosphateHCID 8624045779%

Reaktionsschritte

A solution of 225 (1.17 g, 3.02 mmol) in MeOH (30 mL) with Pd/C (5%, 0.21 g) was hydrogenated at 50 psi for 2.5 h. The mixture was filtered through Celite, washing with MeOH, and the filtrate was evaporated. The residue was dissolved in CH2Cl and the solution was filtered once more, then evaporated to give 2-aminoethyl di(tert-butyl) phosphate (226) (604 mg, 79%) as a colourless oil: 1H NMR [CDCl3] δ 4.01-3.94 (m, 2H), 2.96-2.90 (m, 2H), 1.58 (br s, 2H), 1.49 (s, 18H). HRMS (FAB) calcd. for C10H25NO4P (MH+) m/z 254.1521, found 254.1519.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07718688B2
Quelldatensatzuspto-grants-2010_05
ORD IDord-1822e72c026842a18ad49259fc79ee86
Quellennotizuspto-grants-2010_05