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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593724Generated: November 1, 2026

2,2,2-Trifluoroethanol → HCID 65815868, compound

https://huagongshe.com/reaction/593724

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Chloro-5-iodopyrimidineHCID 11230204—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 65815868HCID 65815868—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2,2,2-trifluoroethanol (0.672 mL, 9.36 mmol) in THF (18.08 mL) was added, portion wise, at 0° C., NaH (0.424 g, 10.61 mmol). The reaction mixture was stirred at 0° C. for 30 min. Then 4-chloro-5-iodopyrimidine (1.5 g, 6.24 mmol) was added and the reaction mixture was refluxed for about 1 hr. The reaction mixture was allowed to cool to room temperature, then a saturated aqueous solution of NH4Cl was added. The mixture was diluted with EtOAc and the layers were separated. The aqueous phase was extracted with EtOAc (2×). The combined organics were washed with brine (1×), dried over Na2SO4, filtered, and concentrated in vacuo to afford the title compound as a yellow solid. ESI MS (M+H)+=304.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242967B2
Source datasetuspto-grants-2016_01
ORD IDord-7e66b82335694cf0a0d7c8c77be3aeb1
Source noteuspto-grants-2016_01