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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256252생성일: 2026년 10월 24일

Magnesium → N-Boc-2-amino-2-methyl-4-(2,2,5,5-tetramethyl-1-cyclopentyl)butene

https://huagongshe.com/ko/reaction/256252

반응식

참여 물질

역할이름HCID투입량
반응물MagnesiumHCID 5462224—
반응물2,2,5,5-Tetramethyl-1-cyclopentylmethylbromideHCID 13629261—
반응물tert-butyl N-(2-methyl-1-oxopropan-2-yl)carbamateHCID 14578674—
용매Diethyl EtherHCID 3283—
생성물N-Boc-2-amino-2-methyl-4-(2,2,5,5-tetramethyl-1-cyclopentyl)buteneHCID 70445521—

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 beings to form. The remainder of the alkyl bromide is then added and the mixture is stirred until all of the magnesium has dissolved. At 0° C. a solution of N-Boc-2-amino-2-methylpropanal 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 dissolves 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 extracted with ether. The organic layer is dried over MgSO4 and evaporated to give N-Boc-2-amino-2-methyl-4-(2,2,5,5-tetramethyl-1-cyclopentyl)butene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04701552
출처 데이터셋uspto-grants-1987_10
ORD IDord-80bc5b99725c46fcbfced3188e09e587
출처 메모uspto-grants-1987_10