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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647416Generated: November 1, 2026

Trifluoroacetic acid → 4,6-Di-tert-butyl-5-hydroxypyrimidine-2-carbaldehyde

https://huagongshe.com/reaction/1647416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
Reactant4,6-Bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)methoxy]-2-pyrimidine carboxaldehydeHCID 19922992—
SolventDichloromethaneHCID 6344—
Product4,6-Di-tert-butyl-5-hydroxypyrimidine-2-carbaldehydeHCID 1529489633%

Reaction Steps

Trifluoroacetic acid (1.05 g, 9.2 mmol) is added to a solution of 4,6-bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)methoxy]-2-pyrimidine carboxaldehyde (1.0 g, 3.1 mmol) in methylene chloride and the reaction mixture is stirred at room temperature for 5 hours. The reaction mixture is neutralized by the addition of saturated aqueous NaHCO3 and the layers separated. The organic layer is washed with brine (50 mL), dried over MgSO4, and evaporated. Recrystallization of the residue from hexane gives pure 4,6-bis(1,1-dimethylethyl)-5-hydroxy-2-pyrimidine carboxaldehyde(0.24 g, 33% ); mp 187°-189° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05432181
Source datasetuspto-grants-1995_07
ORD IDord-5bc40aa6822c440aa550db382724c568
Source noteuspto-grants-1995_07