戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 32294作成日:2026年10月25日

Water → tert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamate

https://huagongshe.com/reaction/32294

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物L-Leucine, N-((1,1-dimethylethoxy)carbonyl)-HCID 83170—
反応物Potassium bisulfateHCID 516920—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒Diethyl EtherHCID 3283—
生成物tert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamateHCID 104275—

反応手順

The Weinreb amide of BocLeucine was dissolved in dry Et2O and added by cannula to an Et2O suspension of an equimolar amount of LiAlH4 at 0° C. After stirring for one hour, the reaction flask was removed from 0° C. and allowed to warm to room temperature. After a reaction time of 80 minutes, an aqueous solution of KHSO4, (2 equiv. of KHSO4, 5 ml H2O/mmol of Weinreb amide) was added slowly while stirring. The aqueous phase was extracted with Et2O and the confined Et2O phases were washed with 3N HCl, saturated NaHCO3, and saturated NaCl. After drying (MgSO4,) and rotary evaporation, the oil was found to contain one compound by thin layer chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427591B2
出典データセットuspto-grants-2008_09
ORD IDord-3c5c784040a64c87816d4340cee56144
出典メモuspto-grants-2008_09