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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1907401생성일: 2026년 10월 26일

t-Butyl 3-(4-bromophenyl)-1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate → t-Butyl 1-(4-bromophenyl)-3-oxohexan-2-ylcarbamate

https://huagongshe.com/reaction/1907401

반응식

참여 물질

역할이름HCID투입량
반응물t-Butyl 3-(4-bromophenyl)-1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamateHCID 18779134—
반응물HCID 178455851HCID 178455851—
용매TetrahydrofuranHCID 8028—
생성물t-Butyl 1-(4-bromophenyl)-3-oxohexan-2-ylcarbamateHCID 6686379156.9%

반응 단계

A solution of propylmagnesium bromide (29.7 g, 201.6 mmol, 3.0 equiv) in THF (200 mL) was added dropwise with stirring at 0° C. to a solution of the carbamate (26 g, 66.5 mmol, 1.0 equiv) in THF (200 mL). The resulting solution was stirred overnight at room temperature. The reaction was then quenched by the addition of aqueous NH4Cl (200 mL). The resulting solution was extracted with EtOAc and the organic layers combined. The resulting mixture was washed with saturated NaHCO3 (200 mL) and saturated aqueous NaCl (200 mL), then dried over anhydrous MgSO4. The residue was applied onto a silica gel column with petroleum ether/EtOAc (5:1) to yield t-butyl 1-(4-bromophenyl)-3-oxohexan-2-ylcarbamate (14 g) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08598170B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-94c4131c90f641b39da909f35edc7472
출처 메모uspto-grants-2013_12