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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746066Generated: October 25, 2026

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

https://huagongshe.com/reaction/746066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantEthyl bromoacetateHCID 7748—
ReactantTriethylamineHCID 8471—
Reactant4-Phenylbutylphosphonous acidHCID 13274665—
SolventChloroformHCID 6212—
Product[Hydroxy-(4-phenylbutyl)phosphinyl]acetic acid, ethyl esterHCID 1335988699.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04602092
Source datasetuspto-grants-1986_07
ORD IDord-d53e219db97841eab7ac8ba22da18f43
Source noteuspto-grants-1986_07