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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 561785Erstellt: 25. Oktober 2026

Acetyl chloride → N-(3-Bromobenzyl)-N-methylacetamide

https://huagongshe.com/reaction/561785

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetyl chlorideHCID 6367—
EduktDiisopropylethylamineHCID 81531—
EduktBenzenemethanamine, 3-bromo-N-methyl-HCID 457588—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-(3-Bromobenzyl)-N-methylacetamideHCID 57956102—

Reaktionsschritte

To a DMF (0.1 M) solution of 3-bromo-N-methylbenzylamine (1 eq.), Hunig's base (3 eq) and 4-(dimethylamino)pyridine (5% loading) was added acetyl chloride (1.5 eq). The resulting reaction mixture was stirred at RT for 16 h. After quenching the reaction with sat. aq. NaHCO3, the mixture was extracted with EtOAc. The organic extract was washed with 10% aq. HCl, sat. aq. NaHCO3, and brine. Drying over Na2SO4, filtration and concentration of the filtrate in vacuo afforded the crude product as a yellow oil. Purification by way of flash chromatography (SiO2, 4:1 (v/v) Hex:EtOAc→EtOAc) afforded the title compound as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063105B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-249c480083964669afc97ff8a33b281e
Quellennotizuspto-grants-2011_11