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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 448863Erstellt: 24. Oktober 2026

Potassium Carbonate → 4-[2-(3-Bromo-4-chloro-benzoylamino)-3-methyl-phenoxy]-butyric acid tert-butyl ester

https://huagongshe.com/de/reaction/448863

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukttert-Butyl 4-bromobutanoateHCID 2757253—
Edukt3-bromo-4-chloro-N-(2-hydroxy-6-methyl-phenyl)-benzamideHCID 68602857—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-[2-(3-Bromo-4-chloro-benzoylamino)-3-methyl-phenoxy]-butyric acid tert-butyl esterHCID 6860251563,6%

Reaktionsschritte

A mixture of 3-bromo-4-chloro-N-(2-hydroxy-6-methyl-phenyl)-benzamide (11.3 g, 33.2 mmol), t-butyl 4-bromobutyrate (8.2 g, 36.6 mmol) and K2CO3 (9.2 g, 66.5 mmol) was heated in DMF (100 mL) at 60° C. for 14 hrs. The mixture was then concentrated to remove DMF and partitioned between ethyl acetate and water. The organic layer was separated and washed with water and brine, dried over MgSO4, then purified by silica gel column chromatography eluting with ethyl acetate/hexane (1/4) to yield a red solid, which was further washed with ether to produce a white powder as 4-[2-(3-bromo-4-chloro-benzoylamino)-3-methyl-phenoxy]-butyric acid tert-butyl ester (10.2 g). MS [M-(t-Bu)+H]+: 425.8/427.8; tR=2.79 min. (method 1)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08481738B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-dddc61b4f6684b5387f8128a96133a13
Quellennotizuspto-grants-2013_07