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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64453생성일: 2026년 10월 27일

Water → methyl 2-(3-{(1S)-1-[(tert-butoxycarbonyl)amino]ethyl}phenyl)-2-methylpropanoate

https://huagongshe.com/reaction/64453

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DimethylformamideHCID 6228—
반응물Silane, ((1-methoxy-2-methyl-1-propenyl)oxy)trimethyl-HCID 552336—
반응물(S)-N-Boc-1-(3-bromophenyl)ethylamineHCID 56971804—
촉매Zinc(II) fluorideHCID 10129912—
촉매HCID 178418851HCID 178418851—
용매Ethyl AcetateHCID 8857—
생성물methyl 2-(3-{(1S)-1-[(tert-butoxycarbonyl)amino]ethyl}phenyl)-2-methylpropanoateHCID 86713467—

반응 조건

온도100 °C

반응 단계

A mixture of 1 g of tert-butyl[(1S)-1-(3-bromophenyl)ethyl]carbamate, 18 mg of bis(tri-tert-butylphosphine)palladium (0), 180 mg of zinc fluoride, 1 ml of [(1-methoxy-2-methylpropa-1-en-1-yl)oxy](trimethyl)silane, and 10 ml of DMF was stirred at 80° C. overnight and at 100° C. for 5 hours. 25 mg of bis(tri-tert-butylphosphine)palladium (0) and 0.34 ml of [(1-methoxy-2-methylpropa-1-en-1-yl)oxy](trimethyl)silane were added thereto, followed by stirring at 80° C. for 3 days. To the reaction mixture were added water and ethyl acetate to carry out a layer separation operation. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 281 mg of methyl 2-(3-{(1S)-1-[(tert-butoxycarbonyl)amino]ethyl}phenyl)-2-methylpropanoate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447090B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-647d358395324543b17b84fbbf089926
출처 메모uspto-grants-2016_09