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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238881Erstellt: 26. Oktober 2026

Triethylamine → 4-fluoro-3-hydroxy-N-methoxy-N-methylbenzamide

https://huagongshe.com/reaction/238881

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
EduktMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Edukt4-Fluoro-3-hydroxybenzoic acidHCID 593635—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-fluoro-3-hydroxy-N-methoxy-N-methylbenzamideHCID 5945905274,1%

Reaktionsbedingungen

Temperatur78 °C

Reaktionsschritte

To a 5 L four necked round bottom flask was added 3-hydroxy-4-fluorobenzoic acid (100 g, 0.64 mol) and CH2Cl2 (2.3 L). Triethylamine (107 mL, 0.768 mol) was then added to the suspension. The solution was cooled to 78° C., and EDCI (184.2 g, 0.961 mol) was added portion wise followed by the addition of N,O-dimethylhydroxyamine hydrochloride (93.6 g, 0.96 mol). The reaction mixture was stirred at −78° C. for 1 h and then allowed to warm to 0° C. over a period of 2 h. The reaction mixture was transferred to a separatory funnel and washed water (2×1.2 L). The organic portion was dried over Na2SO4, filtered and concentrated in vacuo to give 4-fluoro-3-hydroxy-N-methoxy-N-methylbenzamide as a white solid (94.4 g, 74%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642576B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-6d9df3936e90440e83792b9d6c12401f
Quellennotizuspto-grants-2014_02