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HRID 256252Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMagnesiumHCID 5462224—
Edukt2,2,5,5-Tetramethyl-1-cyclopentylmethylbromideHCID 13629261—
Edukttert-butyl N-(2-methyl-1-oxopropan-2-yl)carbamateHCID 14578674—
LösungsmittelDiethyl EtherHCID 3283—
ProduktN-Boc-2-amino-2-methyl-4-(2,2,5,5-tetramethyl-1-cyclopentyl)buteneHCID 70445521—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04701552
Quelldatensatzuspto-grants-1987_10
ORD IDord-80bc5b99725c46fcbfced3188e09e587
Quellennotizuspto-grants-1987_10