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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5582Erstellt: 23. Oktober 2026

o-Chlorophenylacetic acid → Acetyl chloride, 2-(2-chlorophenyl)-

https://huagongshe.com/de/reaction/5582

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukto-Chlorophenylacetic acidHCID 17124—
EduktThionyl ChlorideHCID 24386—
ProduktAcetyl chloride, 2-(2-chlorophenyl)-HCID 182669—

Reaktionsschritte

To 2-chlorophenylacetic acid (0.44 g) is added thionyl chloride (15 ml), and the mixture is stirred at room temperature for 2 hours. Thionyl chloride is distilled off, and the resultant is further distilled off by subjecting twice to azeotrophy with toluene. The resulting residue is dissolved in dichloromethane (10 ml). Separately, to a solution of 5-dimethylamino-1-(4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine (0.40 g) in dichloromethane is added triethylamine (0.36 ml) under ice-cooling, and thereto is added dropwise the above obtained 2-(2-chlorophenyl)acetyl chloride solution. After addition, the mixture is stirred at room temperature for one hour, washed twice with water, dried over magnesium sulfate, and concentrated. The resulting residue is purified by silica gel column chromatography (eluent; chloroform:methanol=200:1), and recrystallized from methanol/diethyl ether to give 5-dimethylamino-1-{4-[2-(2-chlorophenyl)acetylamino]benzoyl}-2,3,4,5-tetrahydro-1H-benzazepine (0.29 g) as white powder, mp. 187°-189° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244898
Quelldatensatzuspto-grants-1993_09
ORD IDord-3db121cfac504d159b1b06562cabf306
Quellennotizuspto-grants-1993_09