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HRID 16821作成日:2026年10月25日

Acetic Acid → tert-Butyl 4-cyclopropylpiperazine-1-carboxylate

https://huagongshe.com/reaction/16821

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物tert-Butyl 4-cyclopropylpiperazine-1-carboxylateHCID 2029452468.3%

反応条件

温度60 °C

反応手順

A solution of tert-butyl piperazine-1-carboxylate (9.31 g, 50 mmol), [(1-ethoxycyclopropyl)oxy]trimethylsilane (20.11 mL, 100.00 mmol) and acetic acid(14.31 mL, 250.00 mmol) in tetrahydrofuran (100 mL), methanol (10 mL) was treated with sodium cyanoborohydride (4.71 g, 75.00 mmol) at 20° C. The resulting solution was stirred at 60° C. for 18 h. The reaction mixture was cooled, filtered and evaporated to dryness. 1N HCl (40 ml) and water (60 ml) were added and the solution extracted with ethyl acetate (3×50 ml). The aqueous layer was basified to pH 10 with solid potassium carbonate and extracted with ethyl acetate (4×50 ml). The organic extracts were washed with saturated sodium chloride solution (50 ml) and dried over MgSO4, filtered and evaporated to dryness to give tert-butyl 4-cyclopropylpiperazine-1-carboxylate (7.73 g, 68.3%) as a white waxy solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737149B2
出典データセットuspto-grants-2010_06
ORD IDord-96114825bb9d43c79c23579a8e9e0a18
出典メモuspto-grants-2010_06