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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | Ethyl 5,6-Dichloronicotinate | HCID 16762519 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 5-chloro-6-(2,2,2-trifluoroethoxy)nicotinate | HCID 86730207 | 92.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09434719B2 |
|---|
| Source dataset | uspto-grants-2016_09 |
|---|
| ORD ID | ord-45a32a935ddc4df1a4e0d16c03d5c2e1 |
|---|
| Source note | uspto-grants-2016_09 |
|---|