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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451556Generated: October 31, 2026

Chlorotrimethylsilane → Ethyl 3-(benzyl(3-ethoxy-3-oxopropyl)amino)-2,2-difluoropropanoate

https://huagongshe.com/reaction/451556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantEthyl bromodifluoroacetateHCID 69585—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(Benzotriazol-1-ylmethylbenzylamino)propionic acid ethyl esterHCID 59442733—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(benzyl(3-ethoxy-3-oxopropyl)amino)-2,2-difluoropropanoateHCID 5944274599.4%

Reaction Steps

To a suspension of activated zinc dust (4.13 g, 63.2 mmol) in dry THF (100 mL) under argon was added TMS-Cl (3.60 g, 4.24 mL, 33.2 mmol). After 10 minutes ethyl bromodifluoroacetate (7.05 g, 4.49 mL, 34.7 mmol) was added slowly, whereby the temperature was kept below 30° C. (cooling with a waterbath). Then a solution of 3-(benzotriazol-1-ylmethyl-benzyl-amino)-propionic acid ethyl ester (10.69 g, 31.6 mmol) in dry THF (100 mL) was added. The exothermic reaction was kept between 20 and 25° C. with a waterbath. The reaction mixture was stirred at room temperature for 12 hours. The reaction mixture was poured on 5% aqueous NaHCO3 solution and filtered over dicalite. The filtrate was extracted three times with ethyl acetate. The organic layers were washed with water and 1 N HCl, then dried over Na2SO4, filtered and the solvents were evaporated. The residue was purified by flash chromatography (silica gel, 100 g, 0% to 50% EtOAc in heptane) to give the title compound as colorless liquid (10.78 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486967B2
Source datasetuspto-grants-2013_07
ORD IDord-3382ecc366394f04b9c4a8799eb5972f
Source noteuspto-grants-2013_07