Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 234839Erstellt: 25. Oktober 2026

Methane → Methyl 5-[(2-chloro-alpha,alpha,alpha-trifluoro-p-tolyl)oxy]salicylate

https://huagongshe.com/reaction/234839

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethaneHCID 297—
EduktHydrochloric AcidHCID 313—
EduktAmmonium HydroxideHCID 14923—
Edukt5-[(2-Chloro-alpha,alpha,alpha-trifluoro-p-tolyl)oxy]salicylic acidHCID 86750233—
LösungsmittelMethanolHCID 887—
LösungsmittelMethanol--water (1/1)HCID 22242641—
ProduktMethyl 5-[(2-chloro-alpha,alpha,alpha-trifluoro-p-tolyl)oxy]salicylateHCID 86750234—

Reaktionsschritte

A chilled solution of 5-[(2-chloro-α,α,α-trifluoro-p-tolyl)oxy]salicylic acid (148 g, 0.45 mol) in methanol is saturated with hydrogen chloride gas, warmed to and held at room temperature overnight and poured onto ice. The aqueous mixture is adjusted to about pH 7.5 with concentrated ammonium hydroxide solution and extracted with methylene chloride. The combined organic extracts are washed with saturated sodium bicarbonate solution, dried over anhydrous sodium sulfate, treated with 10 g of silica gel, filtered and concentrated in vacuo to obtain a dark gum. The gum is dissolved in a methanol-water solution, treated with charcoal, filtered and crystallized to give the title product as an offwhite solid (102.3 g 66.2% mp 62°-64° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05596124
Quelldatensatzuspto-grants-1997_01
ORD IDord-d9843dcd462242bd95e84e2bf8b0d39d
Quellennotizuspto-grants-1997_01