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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-4-fluoropyridine | HCID 2782792 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 4-(Boc-amino)-3-fluoro-phenol | HCID 44185703 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 118223438 | HCID 118223438 | 79.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359338B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-c8881961704c4ec3828ecfd84630b876 |
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| Source note | uspto-grants-2016_06 |
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