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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271712Generated: October 26, 2026

Triethylamine → 4-(2-oxo-2H-pyridin-1-yl)-benzaldehyde

https://huagongshe.com/reaction/1271712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium SulfateHCID 24436—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 18453190HCID 18453190—
SolventTetrahydrofuranHCID 8028—
Product4-(2-oxo-2H-pyridin-1-yl)-benzaldehydeHCID 1070314961%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 4-(2-oxo-2H-pyridin-1-yl)-benzoic acid (0.31 g, 1.4 mmol) in THF (12 mL) was added Et3N (0.30 mL, 2.15 mmol, 1.5 eq) followed by dropwise addition of ClCOOEt (0.16 mL, 1.2 eq) at 0° C. under N2. The mixture was stirred for 1 h at 0° C., filtered, and rinsed with THF. The THF solution was stirred at 0° C., MeOH (3 mL) was added followed by portionwise addition of NaBH4 (0.26 g, 6.8 mmol). The mixture was stirred at 0° C. for 20 min, sat'd Na2SO4 added, extracted with CH2Cl2, dried (MgSO4), filtered, and concentrated to dryness to give 4-(2-oxo-2H-pyridin-1-yl)-benzaldehyde (0.17 g) as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205318B2
Source datasetuspto-grants-2007_04
ORD IDord-404e8cac77324a79bf87521223e5956a
Source noteuspto-grants-2007_04