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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497516Generated: October 29, 2026

Sodium Bicarbonate → HCID 90282035, compound

https://huagongshe.com/reaction/1497516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantGlycine tert-butyl ester hydrochlorideHCID 2725036—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantEthyl 6-formylpyridine-2-carboxylateHCID 44206644—
SolventAcetic AcidHCID 176—
Solvent1,1-DichloroethaneHCID 6365—
SolventTriethylamineHCID 8471—
ProductHCID 90282035HCID 9028203599%

Reaction Steps

To a solution of ethyl 6-formylpyridine-2-carboxylate (1.74 g) in dichloroethane (30.0 mL) were added tert-butyl glycinate hydrochloride (4.89 g), triethylamine (4.06 mL), and acetic acid (2.78 mL), and sodium triacetoxyborohydride (6.18 g) under ice-cooling. The reaction suspension was stirred at room temperature overnight. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution, and then sodium hydrogen carbonate was added thereto until the solution became basic. The reaction mixture was extracted with chloroform, and the organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane-ethyl acetate) to obtain ethyl 6-{[(2-tert-butoxy-2-oxoethyl)amino]methyl}pyridine-2-carboxylate (2.83 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199927B2
Source datasetuspto-grants-2015_12
ORD IDord-e5bc7a3b84314ca09547d2c2726b2d88
Source noteuspto-grants-2015_12