Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1816582Erstellt: 26. Oktober 2026

N-bromobutanimide → Tert-butyl (5-bromo-2-methoxybenzyl)carbamate

https://huagongshe.com/reaction/1816582

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
EduktTert-butyl (2-methoxybenzyl)carbamateHCID 22926021—
LösungsmittelAcetonitrileHCID 6342—
ProduktTert-butyl (5-bromo-2-methoxybenzyl)carbamateHCID 2292603086,6%

Reaktionsschritte

6.04 g of tertiary butyl N-(2-methoxybenzyl)carbamate was dissolved in 50 ml acetonitrile, followed by adding 4.6 g of N-bromosuccinimide thereto. After stirring at room temperature for 3 hours, the solvent was evaporated. The residue was dissolved in ethyl acetate and successively-washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate and the solvent was evapoarated. The residue was washed with a mixture of methyl tertiary butyl methyl ether and hexane, to give 6.97 g of tertiary butyl N-(5-bromo-2-methoxybenzyl)carbamate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06884821B1
Quelldatensatzuspto-grants-2005_04
ORD IDord-f64ec6f64a6e490089b7f086cb208991
Quellennotizuspto-grants-2005_04