Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042043Generated: November 3, 2026

5-Amino-2-chloro-4-fluorophenol → 5-(5-Amino-2-chloro-4-fluorophenoxy)picolinonitrile

https://huagongshe.com/reaction/2042043

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-2-chloro-4-fluorophenolHCID 158654—
Reactant5-Chloro-2-cyanopyridineHCID 3833942—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product5-(5-Amino-2-chloro-4-fluorophenoxy)picolinonitrileHCID 67254079—

Reaction Steps

A solution of 5-amino-2-chloro-4-fluorophenol (100 mg, 0.619 mmol) in degassed dimethylacetamide (2 mL) was treated with potassium t-butoxide (83 mg, 0.743 mmol) and 5-chloro-2-cyanopyridine (86 mg, 0.619 mmol). The resultant mixture was heated to 80° C. overnight, then cooled to RT and diluted with water (10 mL). The mixture was extracted with EtOAc (30 mL). The organic phase was washed with water (3×30 mL) and brine (30 mL) dried (Na2SO4) and concentrated in vacuo to provide 5-(5-amino-2-chloro-4-fluorophenoxy)picolinonitrile as a dark oil which was used without further purification. MS (ESI) m/z: 264.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586565B2
Source datasetuspto-grants-2013_11
ORD IDord-bc20acba90dd4f6ab8e5be468a08a14e
Source noteuspto-grants-2013_11