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HRID 1948038作成日:2026年10月25日

2-(4-Nitrobenzyl)-1,3,2-dioxaphosphinane 2-oxide → 2-(4-Aminobenzyl)-1,3,2-dioxaphosphorinane-2-oxide

https://huagongshe.com/reaction/1948038

反応式

関与物質

役割名称HCID仕込み量
反応物2-(4-Nitrobenzyl)-1,3,2-dioxaphosphinane 2-oxideHCID 11345893—
触媒PalladiumHCID 23938—
溶媒TetrahydrofuranHCID 8028—
生成物2-(4-Aminobenzyl)-1,3,2-dioxaphosphorinane-2-oxideHCID 1129911381.5%

反応条件

温度50 °C

反応手順

To a solution of 2-(4-nitrobenzyl)-1,3,2-dioxaphosphinane 2-oxide (Compound 230D, 70 mg, 0.27 mmol) in anhydrous THF was added 10% Pd/C (10 mg). The resulting mixture was heated at 50° C. under 50 psi H2 atmosphere for 6 h. Catalyst was filtered off and the filtrate was concentrated to give the desired product (50 mg, yield: 80%). 1H NMR (CD3OD, 400 MHz): δ=1.72-1.76 (m, 1H), 1.98-2.02 (m, 1H), 3.19 (d, J=20.4 Hz, 2H), 4.28-4.40 (m, 4H), 6.68 (d, J=8.0 Hz, 2H), 7.03 (d, J=8.4 Hz, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08399433B2
出典データセットuspto-grants-2013_03
ORD IDord-1eabd93c5625442988bda0312fb2fd4d
出典メモuspto-grants-2013_03