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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 387416Erstellt: 25. Oktober 2026

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/387416

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktt-Butyl 3-(4-bromophenyl)-1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamateHCID 18779134—
EduktHCID 178455851HCID 178455851—
LösungsmittelTetrahydrofuranHCID 8028—
Produktt-Butyl 1-(4-bromophenyl)-3-oxohexan-2-ylcarbamateHCID 6686379156,9%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08372984B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-cabb7e9312514dc5a0911d625ab20199
Quellennotizuspto-grants-2013_02