HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497516Generated: October 29, 2026
Sodium Bicarbonate → HCID 90282035, compound
https://huagongshe.com/reaction/1497516
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Glycine tert-butyl ester hydrochloride | HCID 2725036 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Ethyl 6-formylpyridine-2-carboxylate | HCID 44206644 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 90282035 | HCID 90282035 | 99% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09199927B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-e5bc7a3b84314ca09547d2c2726b2d88 |
|---|
| Source note | uspto-grants-2015_12 |
|---|