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HRID 1907401作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物t-Butyl 3-(4-bromophenyl)-1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamateHCID 18779134—
反応物HCID 178455851HCID 178455851—
溶媒TetrahydrofuranHCID 8028—
生成物t-Butyl 1-(4-bromophenyl)-3-oxohexan-2-ylcarbamateHCID 6686379156.9%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08598170B2
出典データセットuspto-grants-2013_12
ORD IDord-94c4131c90f641b39da909f35edc7472
出典メモuspto-grants-2013_12