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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 485563Erstellt: 24. Oktober 2026

Potassium Acetate → 2-Bromo-3-nitrobenzyl acetate

https://huagongshe.com/de/reaction/485563

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium AcetateHCID 517044—
Edukt2-Bromo-1-bromomethyl-3-nitrobenzeneHCID 11066342—
KatalysatorTetrabutylammonium ChlorideHCID 70681—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Bromo-3-nitrobenzyl acetateHCID 1285305251,1%

Reaktionsschritte

A stirred solution of 2-bromo-1-bromomethyl-3-nitrobenzene (20.2 g, 0.0685 mole), potassium acetate (10.08 g, 0.103 mole), and tetrabutylammonium chloride (1.5 g) in 150 ml of acetonitrile was heated at reflux for six hours. The reaction mixture was cooled, filtered, and extracted with methylene chloride. The extract was evaporated to give a residue which was redissolved in methylene chloride and washed twice with 150 ml portions of saturated aqueous sodium chloride solution. The organic phase was passed through phase separation filter paper and evaporated to give a dark solid. The solid was purified by column chromatography on silica gel, elution with toluene, to give (2-bromo-3-nitrophenyl)methyl acetate as a yellow solid (9.6 g, mp 60°-63°).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04536591
Quelldatensatzuspto-grants-1985_08
ORD IDord-97a9a6e7eac0461b80c6b1e62078f6e4
Quellennotizuspto-grants-1985_08