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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 433961Erstellt: 25. Oktober 2026

Toluene → N-Ethyl-3-hydroxy-N-isopropyl-5-methylbenzamide

https://huagongshe.com/reaction/433961

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktSodium HydroxideHCID 14798—
EduktPivaloyl chlorideHCID 62493—
EduktIsopropylethylamineHCID 88318—
LösungsmittelEthanolHCID 702—
LösungsmittelTriethylamineHCID 8471—
ProduktN-Ethyl-3-hydroxy-N-isopropyl-5-methylbenzamideHCID 11172073—

Reaktionsbedingungen

Temperatur2.5 °C

Reaktionsschritte

To a cooled (<5° C.) suspension of 3-hydroxy-5-methylbenzoic acid1 (50 g) in triethylamine (100 g) and toluene (500 ml) under nitrogen, was added pivaloyl chloride (97.2 ml), and the resultant mixture was stirred at 0-5° C. for 2 h. Ethylisopropylamine (55.7 ml) was added, the reaction mixture was stirred at 0-5° C. for 2 h and allowed to reach room temperature. The mixture was washed twice with water and concentrated under reduced pressure to leave a dark oil. This oil was dissolved in ethanol (500 ml) and treated with 5M NaOH solution (100 g of NaOH in 500 ml of water) for 3 h at room temperature. The ethanol was removed under reduced pressure and the resultant basic solution diluted with water and extracted with toluene. The basic layer was acidified with acetic acid to pH5 and the resultant aqueous mixture extracted with dichloromethane. The combined organic extracts were washed with brine and concentrated under reduced pressure to give the title compound as an orange/brown solid (41 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06670381B2
Quelldatensatzuspto-grants-2003_12
ORD IDord-bcebe37f41af4c89bc2413672c7dd1ba
Quellennotizuspto-grants-2003_12