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HRID 2238447作成日:2026年10月26日

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

https://huagongshe.com/reaction/2238447

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl 2-(di-tert-butoxyphosphoryloxy)ethylcarbamateHCID 68635482—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物2-Aminoethyl di(tert-butyl) phosphateHCID 8624045779%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07718688B2
出典データセットuspto-grants-2010_05
ORD IDord-1822e72c026842a18ad49259fc79ee86
出典メモuspto-grants-2010_05