戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 20042作成日:2026年10月25日

Allyl iodide → tert-butyl (S)-2-(allyloxy)-1-((S)-oxiran-2-yl)ethylcarbamate

https://huagongshe.com/reaction/20042

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl iodideHCID 11166—
反応物tert-butyl (S)-2-hydroxy-1-((S)-oxiran-2-yl)ethylcarbamateHCID 86614133—
触媒HCID 178418778HCID 178418778—
溶媒TolueneHCID 1140—
生成物tert-butyl (S)-2-(allyloxy)-1-((S)-oxiran-2-yl)ethylcarbamateHCID 86614132—

反応条件

温度65 °C

反応手順

To a solution of tert-butyl (S)-2-hydroxy-1-((S)-oxiran-2-yl)ethylcarbamate (0.125 g, 0.6 mmol; see: Kurokawa, N.; Ohfune, Y. Tetrahedron 1993, 49, 6195) in toluene (6 mL), was added allyliodide 0.3 mL, 3 mmol) followed by silver(I) oxide (0.7 g, 3 mmol). The solution was stirred at 65° C. in a darkened hood for a period of 15 h. The mixture was then cooled to ambient temperature, filtered through Celite, washed with CH2Cl2, and conc. in vacuo. Purification on SiO2 (10-20% EtoAc/Hexanes) gave the title compound as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745484B2
出典データセットuspto-grants-2010_06
ORD IDord-71e22a70ba924d01bbdb8094577fa4cf
出典メモuspto-grants-2010_06