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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1017808Erstellt: 25. Oktober 2026

Triethylamine → Benzanilide

https://huagongshe.com/reaction/1017808

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
EduktBenzyl p-aminobenzoateHCID 98488—
Edukt1,4-Benzenedicarboxylic acid, methyl esterHCID 3614454—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
ProduktBenzanilideHCID 7168134,8%

Reaktionsschritte

A solution of mono-methyl terephthalate (4.00 g, 22 mmol) in ethyl acetate (25 mL) and DMF (0.1 mL) was cooled in an ice bath and treated with oxalyl chloride (11 mL, 2N in CH2Cl2, 22 mmol) over 30 minutes. After stirring 2 hours at room temperature the solvent was removed on a rotary evaporator and the residue dissolved in CH2Cl2 (20 mL) and added to a solution of benzyl 4-aminobenzoate (5.00 g, 22 mmol) in CH2Cl2 (25 mL) and triethylamine (4.3 mL, 31 mmol) at −60° C. The reaction mixture was warmed to room temperature for 1 hour and then partitioned between water and ethyl acetate. The ethyl acetate layer was dried over sodium sulfate, filtered, and evaporated. The residue was recrystallized from t-butyl methyl ether to give 5.85 g of compound 8.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06479548B2
Quelldatensatzuspto-grants-2002_11
ORD IDord-9f8d21a2aa104ff597679c335e1f7e44
Quellennotizuspto-grants-2002_11