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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 743697Erstellt: 23. Oktober 2026

Methyl N-methylanthranilate → Methyl 2-(N-bromoacetyl-N-methylamino)benzoate

https://huagongshe.com/de/reaction/743697

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl N-methylanthranilateHCID 6826—
EduktSodium HydroxideHCID 14798—
EduktBromoacetyl bromideHCID 61147—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 2-(N-bromoacetyl-N-methylamino)benzoateHCID 1008536192%

Reaktionsschritte

A solution of bromoacetyl bromide (209 g) in dichloromethane (200 ml) was added dropwise to a cooled (ice bath) solution of methyl N-methylanthranilate (168 g) in dichloromethane (1400 ml). A solution of sodium hydroxide (59 g) in water (400 ml) was added dropwise to this ice cold solution then after addition the reaction mixture was stirred at room temperature for 20 h. The organic phase was separated and washed with 1M hydrochloric acid (500 ml), brine (300 ml), saturated sodium hydrogen carbonate solution (400 ml), dried (Na2SO4) then evaporated to afford the required product as a solid (255 g, 92%). Mp 80°-82° C. 1H NMR (360 MHz, CDCl3) δ 3.23 (3H, s), 3.54 (1H, d, J=11 Hz), 3.60 (1H, d, J=11 Hz), 3.90 (3H, s), 7.40 (1H, d, J=8 Hz), 7.51 (1H, dd, J=8 and 8 Hz), 7.65 (1H, dd, J=8 and 8 Hz), 8.04 (1H, d, J=8 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05556969
Quelldatensatzuspto-grants-1996_09
ORD IDord-eec95826b4f6453a829f8506821d44e8
Quellennotizuspto-grants-1996_09