HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Amino-2-chloro-4-fluorophenol → 5-(5-Amino-2-chloro-4-fluorophenoxy)picolinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Amino-2-chloro-4-fluorophenol | HCID 158654 | — |
| Reactant | 5-Chloro-2-cyanopyridine | HCID 3833942 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 5-(5-Amino-2-chloro-4-fluorophenoxy)picolinonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586565B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-bc20acba90dd4f6ab8e5be468a08a14e |
| Source note | uspto-grants-2013_11 |