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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742605Generated: November 4, 2026

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

https://huagongshe.com/reaction/1742605

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 retool) 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 numberUS05340815
Source datasetuspto-grants-1994_08
ORD IDord-3b6b6a784b3a4188b9dd1b30f3d2b0e2
Source noteuspto-grants-1994_08