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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 746066Erstellt: 26. Oktober 2026

Chlorotrimethylsilane → [Hydroxy-(4-phenylbutyl)phosphinyl]acetic acid, ethyl ester

https://huagongshe.com/reaction/746066

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
EduktEthyl bromoacetateHCID 7748—
EduktTriethylamineHCID 8471—
Edukt4-Phenylbutylphosphonous acidHCID 13274665—
LösungsmittelChloroformHCID 6212—
Produkt[Hydroxy-(4-phenylbutyl)phosphinyl]acetic acid, ethyl esterHCID 1335988699,9%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 4-phenylbutyl phosphonous acid (1.0 g, 0.005 mole) in chloroform (20 ml) was added triethylamine (1.6 ml, 0.011 mole) and the solution was cooled in an ice bath to 0° C. Trimethyl silyl chloride (1.4 ml, 0.011 mole) was added to the above solution dropwise, followed by ethyl bromoacetate (0.84 g, 0.56 ml, 0.011 mole). The ice bath was removed and the mixture stirred at room temperature overnight. The mixture was poured into 10% aqueous HCl (10 ml) and crushed ice HCl (10 ml) and crushed ice (10 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 (1.42 g) was vacuum dried to get 1.42 g (99%) of title compound in the form of an oil. TLC: silica gel, CH2Cl2 :MeOH:HOAc shows one main spot, but elongated, Rf =0.29.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04602092
Quelldatensatzuspto-grants-1986_07
ORD IDord-d53e219db97841eab7ac8ba22da18f43
Quellennotizuspto-grants-1986_07