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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033009Generated: October 30, 2026

Sodium Bicarbonate → 3-[(Benzoxazol-2-yl)methoxy]-5-ethyl-6-methylpyridin-2(1H)-one

https://huagongshe.com/reaction/1033009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantBoronHCID 5462311—
Reactant3-[(Benzoxazol-2-yl)methoxy]-2-methoxy-5-ethyl-6-methylpyridineHCID 10334849—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product3-[(Benzoxazol-2-yl)methoxy]-5-ethyl-6-methylpyridin-2(1H)-oneHCID 45482051.6%

Reaction Steps

3[(Benzoxazol-2-yl)methoxy]-2-methoxy-5-ethyl-6-methylpyridine (140 mg, 0.47 mmol) was dissolved in methylene chloride (5 ml) and cooled in an ice bath under an atmosphere of nitrogen. 1M Boron tribomide (2.3 mL, 2.3 mmol) in hexane was added to this solution and the reaction mixture was allowed to warm to room temperature over a 0.75 hour period. This mixture was re-cooled in an ice bath and saturated aqueous NaHCO3 (5 mL) was added to quench the reaction. The methylene chloride layer was dried (Na2SO4), filtered and evaporated. The residue was triturated with diethyl ether to give 69 mg of crude product. Recrystallization from methanol yielded 60 mg (45%), m.p. 198°-200° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308854
Source datasetuspto-grants-1994_05
ORD IDord-3e0a6ec88a12424795066a833e2c57c6
Source noteuspto-grants-1994_05