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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57452Generated: October 26, 2026

2,2,2-Trifluoroethanol → Ethyl 5-chloro-6-(2,2,2-trifluoroethoxy)nicotinate

https://huagongshe.com/reaction/57452

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantEthyl 5,6-DichloronicotinateHCID 16762519—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-chloro-6-(2,2,2-trifluoroethoxy)nicotinateHCID 8673020792.9%

Reaction Conditions

Temperature-73 °C

Reaction Steps

To a solution of ethyl 5,6-dichloronicotinate (6.28 g, 28.5 mmol) and 2,2,2-trifluoroethanol (2.71 ml, 37.1 mmol) in THF (90 ml) at −73° C. was added NaHMDS (37.1 ml, 37.1 mmol). The reaction was stirred at −73° C. for 30 minutes, then at 0° C. for 5 hours. The reaction was quenched with 30 mL saturated NH4Cl solution. The reaction mixture was then poured into 50 mL brine and phases were separated. The aqueous layer was extracted with DCM (2×100 mL). The combined organics were dried (Na2SO4) and concentrated. Silica gel chromatography with 100% heptane to 30% EtOAc in heptane provided final product (7.51 g). LCMS m/z 284.1 (M+H)+, Rt 1.07 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434719B2
Source datasetuspto-grants-2016_09
ORD IDord-45a32a935ddc4df1a4e0d16c03d5c2e1
Source noteuspto-grants-2016_09