戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 58836作成日:2026年10月24日

Imidazole → methyl (2R)-2-(((tert-butoxy)carbonyl)amino)-3-iodopropanoate

https://huagongshe.com/ja/reaction/58836

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物TriphenylphosphineHCID 11776—
反応物Iodide IonHCID 30165—
反応物N-Boc-L-serine methyl esterHCID 7019177—
溶媒DichloromethaneHCID 6344—
生成物methyl (2R)-2-(((tert-butoxy)carbonyl)amino)-3-iodopropanoateHCID 1090359168.1%

反応条件

温度0 °C

反応手順

A mixture of triphenylphosphine (131 g, 0.500 mol) and imidazole (34 g, 0.50 mol) in DCM (600 mL) was cooled to 0° C. and iodide (127 g, 0.50 mol) was added in small portions over 0.5 h. The cooling bath was removed and the mixture was stirred for 0.5 h. After the mixture was re-cooled to 0° C., a solution of (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate (73 g, 0.33 mol) in DCM (300 mL) was added dropwise. After the addition, the cooling bath was removed and the mixture was allowed to warm to ambient temperature and stirred for 1.5 h. The mixture was filtered and the filtrate was concentrated to remove most of the solvent. MTBE (400 mL) was added to the residue and the mixture was filtered to remove triphenylphosphine oxide. The filtrate was concentrated and the residue was purified by flash column chromatography on silica gel to afford (R)-methyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate (74.0 g, 68% yield) as a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434761B2
出典データセットuspto-grants-2016_09
ORD IDord-c4c62557219c49f4894c4f195aa68a46
出典メモuspto-grants-2016_09