HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488810Generated: October 31, 2026
Dimethylformamide → 6-Methoxypyridine-3-carbaldehyde
https://huagongshe.com/reaction/488810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-Bromo-2-methoxypyridine | HCID 2734895 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 6-Methoxypyridine-3-carbaldehyde | HCID 3364576 | — |
Reaction Steps
To a solution of 5-bromo-2-methoxy-pyridine (8.50 g, 45.2 mmol) in 100 mL dry ether under argon at −64° C. was added 1.6 M n-BuLi in hexanes. The resulting mixture was stirred at −64° C. for 40 minutes and allowed to warm to −35° C. To the resulting suspension was added 7.0 mL of dry DMF over 10 minutes. After 15 minutes, the mixture was allowed to warm to 0° C. and 75 mL of 5% NH4Cl was added. The resulting mixture was separated and the aqueous layer extracted with EtOAc (3×75 mL). The organics were combined, dried (MgSO4), filtered and evaporated under vacuum to give 2-methoxy-pyridine-5-carboxaldehyde as a tannish solid (recrystallized from hexane), 3.76 g (60.6%); m.p. 48.5-50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06974826B2 |
|---|
| Source dataset | uspto-grants-2005_12 |
|---|
| ORD ID | ord-b5f20d3a42754bffada595695a6007c6 |
|---|
| Source note | uspto-grants-2005_12 |
|---|