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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724872Generated: October 31, 2026

Dimethylformamide → tert-Butyl 4-chloro-3-formylpyridin-2-ylcarbamate

https://huagongshe.com/reaction/1724872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactanttert-butyl N-(4-chloropyridin-2-yl)carbamateHCID 1516418—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-chloro-3-formylpyridin-2-ylcarbamateHCID 46204204—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dissolve tert-butyl 4-chloropyridin-2-ylcarbamate (1.95 g, 0.00855 moles) in dry THF (50 mL) and cool to −78° C. under nitrogen atmosphere. Add dropwise 1.6 M n-BuLi/hexane (12.8 mL, 0.02053 moles) over a period of 15 minutes while maintaining the reaction temperature below −70° C. Stir the resulting red orange solution at −78° C. for 2 hours. Add DMF (3.3 mL, 0.04275 moles) dropwise to the reaction mixture while maintaining the reaction temperature below −70° C. Stir further at −78° C. for 2 hours and then quench the reaction mixture with saturated ammonium chloride (50 mL). Warm the reaction mixture to room temperature, extract with EtOAc (3×50 mL) and dry with MgSO4. Filter and concentrate under reduced pressure to afford a yellow viscous oil. Purify the crude product by flash column chromatography using 15-20% EtOAc/hexane to afford the title product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488740B2
Source datasetuspto-grants-2009_02
ORD IDord-b504d4fd05b54c95be18388f816a8c20
Source noteuspto-grants-2009_02