HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277168Generated: November 1, 2026
Methanol → Methyl 6-(cyclopropylmethoxy)-5-fluoronicotinate
https://huagongshe.com/reaction/2277168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Bromo-2-(cyclopropylmethoxy)-3-fluoropyridine | HCID 86715117 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 6-(cyclopropylmethoxy)-5-fluoronicotinate | HCID 86731223 | — |
Reaction Steps
A mixture of 5-bromo-2-(cyclopropylmethoxy)-3-fluoropyridine (2.49 g), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) dichloromethane adduct (832 mg), triethylamine (2.82 mL), methanol (2 mL) and DMF (20 mL) was stirred overnight at 80° C. under a carbon monoxide atmosphere. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (1.75 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09133129B2 |
|---|
| Source dataset | uspto-grants-2015_09 |
|---|
| ORD ID | ord-42e0d4e0829042b6aa5359161b811fac |
|---|
| Source note | uspto-grants-2015_09 |
|---|