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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 78492Erstellt: 24. Oktober 2026

Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) → Methyl 5-chloro-2-(2-chloroethoxy)benzoate

https://huagongshe.com/de/reaction/78492

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanol, 2-chloro-, 1-(4-methylbenzenesulfonate)HCID 6639—
EduktPotassium CarbonateHCID 11430—
EduktBenzoic acid, 5-chloro-2-hydroxy-, methyl esterHCID 77684—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl 5-chloro-2-(2-chloroethoxy)benzoateHCID 66846837—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A mixture of methyl-5-chlorosalicylate (19.5 g, 105 mmol), 2-chloroethyl p-toluenesulfonate (19.3 mL, 107 mmol) and K2CO3 (28.9 g, 210 mmol) in 105 mL of N,N-dimethylformamide was warmed to 50° C. and allowed to stir for 18 hours. The mixture was cooled to ambient temperature, diluted with 25 mL of ethyl acetate and 25 mL of H2O. The layers were separated and the organic layer was dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Purification via column chromatography (SiO2, 75% hexanes in ethyl acetate) afforded the title compound. MS (DCI/NH3) m/z 249 (M+H)+, 266 (M+NH4)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841334B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-191942b1cd1f4610a6c345a57cd8f0b7
Quellennotizuspto-grants-2014_09