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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735802Generated: October 30, 2026

N-bromobutanimide → Ethyl 2-bromo-6-(1,1-dimethylethyl)-3-hydroxy-4-pyridinecarboxylate

https://huagongshe.com/reaction/735802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58980622HCID 58980622—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-bromo-6-(1,1-dimethylethyl)-3-hydroxy-4-pyridinecarboxylateHCID 5898064896%

Reaction Steps

To a solution of the above isonicotinic acid ethyl ester (2.0 g, 9.47 mmol) in DMF (20 mL) was added N-bromosuccinimide (1.85 g, 10.4 mmol). The solution was stirred at room temperature for 0.5 h then poured into saturated aqueous NaHCO3. The aqueous layer was extracted with diethyl ether and the combined organic layers were washed with saturated aqueous NaHCO3, dried over sodium sulfate, filtered, and concentrated in vacuo to provide 2-bromo-6-tert-butyl-3-hydroxy-isonicotinic acid ethyl ester (2.74 g, 96%) as a pale yellow oil which was utilized without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592332B2
Source datasetuspto-grants-2009_09
ORD IDord-81c9bb463bae45d7a92fa3b1b3b274e9
Source noteuspto-grants-2009_09