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HRID 2239528作成日:2026年10月26日

Benzyl 4-(2-(tert-butyldimethylsilyloxy)ethyl)piperazine-1-carboxylate → 1-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)piperazine

https://huagongshe.com/reaction/2239528

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl 4-(2-(tert-butyldimethylsilyloxy)ethyl)piperazine-1-carboxylateHCID 58812409—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物1-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)piperazineHCID 5829982488%

反応手順

A mixture of benzyl 4-(2-(tert-butyldimethylsilyloxy)ethyl)piperazine-1-carboxylate (Method 90, 2.1 g, 5.55 mmol) and Pd/C (0.059 g, 0.55 mmol) in methanol (30 mL) was stirred under H2 (g) for 24 hours. The reaction mixture was filtered through a pad of Celite and concentrated under reduced pressure to give 1.20 g, (88%) of a yellow oil. 1H NMR: CD3Cl 3.74 (t, 2H), 2.90 (m, 4H), 2.51 (m, 6H), 0.88 (s, 9H), 0.04 (s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07723337B2
出典データセットuspto-grants-2010_05
ORD IDord-598620f990ba4d77a236db01de1f2e4d
出典メモuspto-grants-2010_05