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HRID 256252作成日:2026年10月26日

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

https://huagongshe.com/reaction/256252

反応式

関与物質

役割名称HCID仕込み量
反応物MagnesiumHCID 5462224—
反応物2,2,5,5-Tetramethyl-1-cyclopentylmethylbromideHCID 13629261—
反応物tert-butyl N-(2-methyl-1-oxopropan-2-yl)carbamateHCID 14578674—
溶媒Diethyl EtherHCID 3283—
生成物N-Boc-2-amino-2-methyl-4-(2,2,5,5-tetramethyl-1-cyclopentyl)buteneHCID 70445521—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04701552
出典データセットuspto-grants-1987_10
ORD IDord-80bc5b99725c46fcbfced3188e09e587
出典メモuspto-grants-1987_10