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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2112027Erstellt: 27. Oktober 2026

Triethylamine → Methyl 2-{[4-(3-{4-[(methylsulfonyl)oxy]phenoxy}propyl)phenoxy]methyl}benzoate

https://huagongshe.com/reaction/2112027

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
EduktMethyl 2-({4-[3-(4-hydroxyphenoxy)propyl]phenoxy}methyl)benzoateHCID 68869776—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 2-{[4-(3-{4-[(methylsulfonyl)oxy]phenoxy}propyl)phenoxy]methyl}benzoateHCID 8660192697,3%

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

Methyl 2-({4-[3-(4-hydroxyphenoxy)propyl]phenoxy}methyl)benzoate (0.32 g, 0.81 mmol) was dissolved in dichloromethane (10 ml) and cooled to −20° C. Triethylamine (0.123 g, 1.22 mmol) was added drop wise and methanesulfonyl chloride (0.10 g, 0.89 mmol) was added drop wise. The ice bath was removed and the mixture was wormed to room temperature. Diethyl ether (5 ml) was added and the precipitate was filtered off. The organic phase was washed with two portions of brine (5 ml) and dried (MgSO4). Removing the solvent by evaporation gave 0.37 gram of methyl 2-{[4-(3-{4-[(methylsulfonyl)oxy]phenoxy}propyl)phenoxy]methyl}benzoate (yield 97.3%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07521461B2
Quelldatensatzuspto-grants-2009_04
ORD IDord-4b491a9affc54b0f87b67d5d053935c6
Quellennotizuspto-grants-2009_04