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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1980056Erstellt: 27. Oktober 2026

Benzene → N-(4-fluoro-alpha,alpha-dimethylbenzyl)-o-methylphenylacetamide

https://huagongshe.com/reaction/1980056

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
Edukto-Tolyl-acetyl chlorideHCID 2760632—
Edukt1-(4-Fluorophenyl)-1-methylethylamineHCID 13025665—
LösungsmittelTriethylamineHCID 8471—
ProduktN-(4-fluoro-alpha,alpha-dimethylbenzyl)-o-methylphenylacetamideHCID 1279029678,8%

Reaktionsschritte

Into a 300 ml four-necked flask, there were charged benzene (200 ml), 4-fluoro-α,α-dimethylbenzylamine (7.7 g) and triethylamine (6.0 g), and o-methylphenylacetyl chloride (9.5 g) was dropwise added thereto at room temperature while stirring, followed by refluxing for 3 hours. After cooling, the reaction mixture was washed with water to remove triethylamine hydrochloride. After the benzene layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was recrystallized from ethanol to give 11.3 g of N-(4-fluoro-α,α-dimethylbenzyl)-o-methylphenylacetamide (Compound No. 11). M.P., 150°-151° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04484942
Quelldatensatzuspto-grants-1984_11
ORD IDord-18fc235c6aba47319e43615affca2fd3
Quellennotizuspto-grants-1984_11