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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200115Generated: October 25, 2026

2-Chloro-4-fluoropyridine → HCID 118223438, compound

https://huagongshe.com/reaction/2200115

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-fluoropyridineHCID 2782792—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-(Boc-amino)-3-fluoro-phenolHCID 44185703—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 118223438HCID 11822343879.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolve tert-butyl N-(2-fluoro-4-hydroxy-phenyl)carbamate (10.47 g, 46.1 mmol) in N-methyl-2-pyrrolidone (NMP, 100 mL), add t-BuOK (5.67 g, 50.5 mmol) and stir at 0° C. for 30 min. Add 2-chloro-4-fluoropyridine (5.5 g, 41.9 mmol), then stir at 70° C. under N2 for 12 hrs. Quench the reaction with water, extract with EtOAc (300 mL×3), combine the organic layers, wash with brine (300 mL×2), dry over anhydrous Na2SO4. Concentrate under reduced pressure to give the crude product. Purification by chromatography (silica gel, EtOAc:PE=1:4) affords the title compound (11.23 g, 79.5%). MS: (M+1): 339.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359338B2
Source datasetuspto-grants-2016_06
ORD IDord-c8881961704c4ec3828ecfd84630b876
Source noteuspto-grants-2016_06