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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707978Generated: October 31, 2026

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

https://huagongshe.com/reaction/1707978

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 numberUS05356898
Source datasetuspto-grants-1994_10
ORD IDord-0f8dd9f088b64155b25c63da30bde3c8
Source noteuspto-grants-1994_10