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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58836생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/58836

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물TriphenylphosphineHCID 11776—
반응물Iodide IonHCID 30165—
반응물N-Boc-L-serine methyl esterHCID 7019177—
용매DichloromethaneHCID 6344—
생성물methyl (2R)-2-(((tert-butoxy)carbonyl)amino)-3-iodopropanoateHCID 1090359168.1%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434761B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-c4c62557219c49f4894c4f195aa68a46
출처 메모uspto-grants-2016_09