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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623937Generated: October 29, 2026

Water → Tert-butyl 3-(5-bromopyrimidin-2-yl)oxy-2,2-dimethylpropanoate

https://huagongshe.com/reaction/623937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-2-chloropyridineHCID 2734414—
ReactantTert-butyl 3-hydroxy-2,2-dimethylpropanoateHCID 54272639—
ProductTert-butyl 3-(5-bromopyrimidin-2-yl)oxy-2,2-dimethylpropanoateHCID 67972905—

Reaction Conditions

Temperature50 °C

Reaction Steps

In N,N-dimethylformamide (10 mL) were dissolved 5-bromo-2-chloropyridine (1000 mg) and tert-butyl 3-hydroxy-2,2-dimethylpropanoate (991 mg), and 60% sodium hydride (248 mg) was added to the solution under ice-cooling. The reaction mixture was stirred at room temperature for 6 hours, at 50° C. for 1 hour and 45 minutes, and then, at room temperature overnight. Water was added to the reaction mixture under ice-cooling, and the mixture was extracted with ether. The organic layer was separated, washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=100:0 to 95:5) to obtain tert-butyl 3-(5-bromopyrimidin-2-yl)oxy-2,2-dimethylpropanoate (1.048 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302996B2
Source datasetuspto-grants-2016_04
ORD IDord-61eabace70ee45f9a9f7eb6bdf4c80ca
Source noteuspto-grants-2016_04