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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171255Generated: November 2, 2026

Cesium carbonate → tert-Butyl (2-chloro-5-fluoropyridin-4-yl)carbamate

https://huagongshe.com/reaction/2171255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactanttert-Butyl carbamateHCID 77922—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant2-Chloro-5-fluoro-4-iodopyridineHCID 24820495—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Producttert-Butyl (2-chloro-5-fluoropyridin-4-yl)carbamateHCID 7174153079.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

tert-Butyl carbamate (960 mg), cesium carbonate (5.06 g), Pd2(dba)3 (1.07 g), and Xantphos (1.35 g) were added to a toluene solution (40 ml) containing 2-chloro-5-fluoro-4-iodopyridine (2 g), followed by stirring at 100° C. for 3 hours. The reaction solution was adjusted to room temperature and water was added to the reaction solution, followed by extraction with ethyl acetate. The organic layers were washed with saturated saline and dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure and the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=9:1 to 4:1). A yellow oily matter of tert-butyl (2-chloro-5-fluoropyridin-4-yl)carbamate (1.53 g) was thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051310B2
Source datasetuspto-grants-2015_06
ORD IDord-03c91063e62a4b90ac9c3ff8a207582d
Source noteuspto-grants-2015_06