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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167900Generated: October 30, 2026

Chlorotrimethylsilane → 2,2-Difluoro-3-(2-(4-octyloxy-phenyl)-morpholin-4-yl)-propionic acid ethyl ester

https://huagongshe.com/reaction/2167900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantEthyl bromodifluoroacetateHCID 69585—
Reactant1-[2-(4-octyloxy-phenyl)-morpholin-4-ylmethyl]-1H-benzotriazoleHCID 68193808—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
Product2,2-Difluoro-3-(2-(4-octyloxy-phenyl)-morpholin-4-yl)-propionic acid ethyl esterHCID 67032372—

Reaction Steps

To a suspension of zinc dust (0.34 g; 5.2 mmol) in dry THF (10 mL) was added chlorotrimethylsilane (0.33 mL; 2.6 mmol) and ethyl bromodifluoroacetate (0.50 ml; 3.9 mmol), this mixture was heated under reflux for 10 min. and then cooled to RT. To the resulting mixture was added drop-wise a solution of 1-[2-(4-octyloxy-phenyl)-morpholin-4-ylmethyl]-1H-benzotriazole in THF (5 mL). After the addition is complete the resulting mixture is heated under efflux for 2 hours. After cooling to RT the reaction mixture was filtered over Kieselguhr and the filter-cake was washed with ethanol. The solvents were removed in vacuo and the residue was purified by column chromatography (SiO2, Et2O:hexanes 1:1) to afford 2,2-difluoro-3-(2-(4-octyloxy-phenyl)-morpholin-4-yl)-propionic acid ethyl ester (0.58 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045441B2
Source datasetuspto-grants-2015_06
ORD IDord-36fb642c620148128021902e72b9278c
Source noteuspto-grants-2015_06