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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923480Generated: October 31, 2026

Water → Di-tert-butyl [(3-bromopyridin-4-yl)methyl]imidodicarbonate

https://huagongshe.com/reaction/923480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDi-tert-butyl IminodicarboxylateHCID 279800—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3-Bromo-4-(chloromethyl)pyridineHCID 66933309—
SolventDimethylformamideHCID 6228—
ProductDi-tert-butyl [(3-bromopyridin-4-yl)methyl]imidodicarbonateHCID 11831807490.3%

Reaction Steps

To a solution of 1.73 g of di-tert-butyl imidodicarbonate in DMF 16 ml was added 894 mg of potassium tert-butoxide under ice-cooling, followed by stirring at room temperature for 1 hour. To the reaction mixture was added a solution of 1.37 g of 3-bromo-4-(chloromethyl)pyridine in 3 ml of DMF under ice-cooling, followed by stirring at room temperature for 2 hours. To the reaction mixture was added water, followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was then evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 2.32 g of di-tert-butyl [(3-bromopyridin-4-yl)methyl]imidodicarbonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278968B2
Source datasetuspto-grants-2016_03
ORD IDord-028586114a174a939c375347c41a4ded
Source noteuspto-grants-2016_03