HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Methoxide → 1-Methoxy-6-methyl-5-nitroisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-Chloro-6-methyl-5-nitroisoquinoline | HCID 22622221 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Methoxy-6-methyl-5-nitroisoquinoline | HCID 22622219 | 74% |
Reaction Steps
A stirred solution of 1-chloro-6-methyl-5-nitroisoquinoline (1.2 g, 5.4 mmol) and sodium methoxide (0.6 g, 95%, 11 mmol) in methanol (20 mL) in a sealed-tube was heated to 80° C. for 2 h, cooled to room temperature and partitioned between ethyl acetate (3×30 mL) and water (50 mL). The combined organic extracts were washed (water, brine), dried (sodium sulfate) and concentrated in vacuo to give the product as a beige solid (0.87 g, 74%). A sample recrystallised from ethanol gave mp 94° C.; Found: C, 60.45; H, 4.58; N, 12.74%. C11H10N2O3 requires C, 60.55; H, 4.62; N, 12.83%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06365598B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-997d8b2213a549a383397ef84095e516 |
| Source note | uspto-grants-2002_04 |