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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1428004Erstellt: 26. Oktober 2026

N-bromobutanimide → tert-Butyl 4-(4-amino-3-bromophenyl)-piperidine-1-carboxylate

https://huagongshe.com/reaction/1428004

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Edukttert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylateHCID 21940085—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
Produkttert-Butyl 4-(4-amino-3-bromophenyl)-piperidine-1-carboxylateHCID 56834849103,1%

Reaktionsschritte

To a solution of 4-(4-amino-phenyl)-piperidine-1-carboxylic acid tert-butyl ester (0.20 g, 0.71 mmol) (as prepared in the previous step) in DCM (3 mL) was added N-bromosuccinimide (NBS) (0.13 g, 0.71 mmol), and the reaction stirred at RT for 10 h. The reaction was diluted with EtOAc (10 mL) and washed with NaHCO3 (2×10 mL) and brine (10 mL). Concentration of the organic layer gave 0.26 g (100%) of the title compound as a yellow foam. Mass spectrum (ESI, m/z): Calcd. for C16H23BrN2O2, 355.1 (M+H). found 355.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08933091B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-e9eed31b58604b7aa0224ca0f8d789e4
Quellennotizuspto-grants-2015_01