HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15302Generated: October 25, 2026
Formaldehyde → Methyl 2-[3-chloro-6-(methoxy)-1,5-naphthyridin-4-yl]-2-propenoate
https://huagongshe.com/reaction/15302
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl [3-chloro-6-(methyloxy)-[1,5]naphthyridin-4-yl]acetate | HCID 57707490 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Methyl 2-[3-chloro-6-(methoxy)-1,5-naphthyridin-4-yl]-2-propenoate | HCID 57486868 | 89% |
Reaction Steps
A mixture of methyl[3-chloro-6-(methyloxy)-1,5-naphthyridin-4-yl]acetate (43.3 g, 162 mmol), benzyltriethylammonium chloride (71.2 g, 313 mmol), potassium carbonate (42 g, 304 mmol) and paraformaldehyde (42 g) in cyclohexane (1060 ml) was heated at 80° C. for 24 h, cooled and treated with ethyl acetate and water. After separation, the aqueous was extracted with ethyl acetate. The combined organic phases were dried and the solvent was removed. The residue was subjected to column chromatography on silica gel using hexane/15% ethyl acetate to provide the desired compound (40.2 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07732461B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-8a5f8952a0f6427990cce09d7e945dcd |
|---|
| Source note | uspto-grants-2010_06 |
|---|