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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1731504생성일: 2026년 10월 25일

Diethyl Ether → N-Boc-1-amino-1-(2,2,5,5-tetramethyl-1-cyclopentyl)ethenylcyclopropane

https://huagongshe.com/reaction/1731504

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물MagnesiumHCID 5462224—
반응물(1-Formylcyclopropyl)carbamic acid tert-butyl esterHCID 10352385—
반응물2,2,5,5-Tetramethyl-1-cyclopentylmethylbromideHCID 13629261—
생성물N-Boc-1-amino-1-(2,2,5,5-tetramethyl-1-cyclopentyl)ethenylcyclopropaneHCID 70445455—

반응 단계

A solution of 2,2,5,5-Tetramethyl-1-cyclopentylmethyl bromide in ether is added slowly to magnesium turnings until the Grignard reagent begins to form. The remainder of the alkyl bromide is then added and the mixture is stirred until all the magnesium dissolves. At 0° C. a solution of N-Boc-1-amino-1-cyclopropanecarboxaldehyde is then added and the mixture is stirred overnight. The reaction is quenched with 1M HCl, extracted with ether and the extracts are evaporated. The residue is dissolved in dioxane and 2M H2SO4 is added. The mixture is heated until the alcohol is dehydrated, as shown by thin layer chromatography. Water is added and the mixture is extracted with ether. The organic layer is dried over MgSO4 and evaporated to give N-Boc-1-amino-1-(2,2,5,5-tetramethyl-1-cyclopentyl)ethenylcyclopropane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04622232
출처 데이터셋uspto-grants-1986_11
ORD IDord-48aa57e5e071462eaa2c435edaaf56c7
출처 메모uspto-grants-1986_11