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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132352Generated: October 25, 2026

Triethylamine → N-(3-Formyl-2-pyridinyl)-2,2-dimethylpropanamide

https://huagongshe.com/reaction/132352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
Reactant3-Pyridinecarboxaldehyde, 2-amino-HCID 737633—
SolventDichloromethaneHCID 6344—
ProductN-(3-Formyl-2-pyridinyl)-2,2-dimethylpropanamideHCID 73683790%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethlyamine (7.6 mL, 54 mmol), was added to a solution of 2-aminopyridine-3-carboxaldehyde (4.45 g, 36 mmol) in dichloromethane (70 mL). Mixture was cooled to 0° C. A solution of pivaloyl chloride (5.3 mL, 43 mmol) in dichloromethane (30 mL) was added to the mixture. Reaction was warmed to room temperature. Mixture stirred at room temperature for 63 hours. Mixture was washed successively with water (2×50 mL) and brine (30 mL). Organic layer was dried (magnesium sulfate), filtered and concentrated in vacuo. Silica gel chromatography afforded the title compound as off-white solid in 90% yield. (M+H)+=207.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384931B2
Source datasetuspto-grants-2008_06
ORD IDord-1c58341a15d048099266fe6211fcbb02
Source noteuspto-grants-2008_06