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HRID 4256作成日:2026年10月24日

tert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamate → (3RS,4S)-4-(tert-butoxycarbonyl)amino-6-methylhepten-3-ol

https://huagongshe.com/ja/reaction/4256

反応式

関与物質

役割名称HCID仕込み量
反応物tert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamateHCID 104275—
反応物HCID 178418507HCID 178418507—
溶媒TetrahydrofuranHCID 8028—
生成物(3RS,4S)-4-(tert-butoxycarbonyl)amino-6-methylhepten-3-olHCID 1385604965%

反応手順

To a stirred 0° C. solution of Boc-leucinal (3.00 g, 13.9 mmol) in dry tetrahydrofuran (THF) (70 ml) was added vinyl magnesium bromide (35 ml of a 1.0M solution in THF). After 5 hours, the mixture was quenched with 1.0M NH4Cl (50 ml). Most of the THF was evaporated in vacuo and the residue was extracted with ether several times. The combined extracts were washed (brine), dried (Na2SO4), filtered, and evaporated to give the desired product as a 3:2 mixture of hydroxy diastereomers in 65% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04725583
出典データセットuspto-grants-1988_02
ORD IDord-5281eca835b24f4999f7ce801feb6dce
出典メモuspto-grants-1988_02