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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017707Generated: October 30, 2026

Dimethylformamide → tert-butyl N-(3-formylpyridin-2-yl)carbamate

https://huagongshe.com/reaction/1017707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-(Boc-amino)pyridineHCID 11206349—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
Producttert-butyl N-(3-formylpyridin-2-yl)carbamateHCID 14177125—

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyllithium (1.7 M, 14.5 mL, 24.6 mmol, 2.39 equiv) was added to a solution of pyridin-2-yl-carbamic acid tert-butyl ester (5-1, 2.00 g, 10.3 mmol, 1 equiv) in ethyl ether (100 mL) at −78° C., and the resulting mixture was warmed to 0° C. and stirred for 1 h. N,N-Dimethylformamide (8.00 mL, 103 mmol, 10.0 equiv) was added with rapid stirring. The mixture was stirred at 0° C. for 10 min, then partitioned between half-saturated aqueous ammonium chloride solution (100 mL). The aqueous layer was further extracted with ethyl acetate (100 mL), and the combined organic layers were dried over sodium sulfate and concentrated. The residue was purified by flash column chromatography (40% ethyl acetate in hexanes) to afford (3-formyl-pyridin-2-yl)-carbamic acid tert-butyl ester (5-2) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479512B1
Source datasetuspto-grants-2002_11
ORD IDord-2b6774d61de4477ba679acdc8cef5df7
Source noteuspto-grants-2002_11