Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
t-Butyl 3-(4-bromophenyl)-1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate → t-Butyl 1-(4-bromophenyl)-3-oxohexan-2-ylcarbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | t-Butyl 3-(4-bromophenyl)-1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate | HCID 18779134 | — |
| 반응물 | HCID 178455851 | HCID 178455851 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | t-Butyl 1-(4-bromophenyl)-3-oxohexan-2-ylcarbamate | HCID 66863791 | 56.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09181206B2 |
| 출처 데이터셋 | uspto-grants-2015_11 |
| ORD ID | ord-8a74778347054a6cb65034e4a68a45d3 |
| 출처 메모 | uspto-grants-2015_11 |