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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 746065Erstellt: 26. Oktober 2026

Diethyl Ether → [Ethoxy(4-phenylbutyl)phosphoryl]acetic acid

https://huagongshe.com/reaction/746065

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktBromoacetic AcidHCID 6227—
EduktChlorotrimethylsilaneHCID 6397—
EduktTriethylamineHCID 8471—
Edukt4-Phenylbutylphosphonous acidHCID 13274665—
LösungsmittelChloroformHCID 6212—
Produkt[Ethoxy(4-phenylbutyl)phosphoryl]acetic acidHCID 1313684897%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 4-phenylbutyl phosphonous acid, ethyl ether (0.5 g, 0.0022 mole) in chloroform (10 ml) was added triethylamine (0.68 ml, 0.0048 mole) and the solution was cooled in an ice bath to 0° C. Trimethyl silyl chloride (0.6 ml, 0.0048 mole) was added to the above solution dropwise, followed by bromoacetic acid (0.34 g, 0.0024 mole). The ice bath was removed and the mixture stirred at room temperature for 5 hours and poured into 10% aqueous HCl (30 ml) and crushed ice (20 g). After shaking the mixture in a separatory funnel, the chloroform layer was separated and the aqueous layer extracted with dichloromethane (2×50 ml). The combined organic phase was washed with brine, dried over anhydrous sodium sulfate and the solvents removed on a rotavap. The resulting crude thick oil was vacuum dried to get 0.61 g (97%) of title compound in the form of an oil, TLC: Silica gel, CH2Cl2 :MeOH:HOAc shows one main spot at Rf =0.37.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04602092
Quelldatensatzuspto-grants-1986_07
ORD IDord-1f460e3036be4135ae4478e6628ba798
Quellennotizuspto-grants-1986_07