Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1H-Pyrazole, 3-(bromomethyl)-5-chloro-1-methyl-4-nitro- | HCID 10264316 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Product | HCID 21250760 | HCID 21250760 | 40% |
Reaction Steps
A solution of 3-bromomethyl-5-chloro-1-methyl-4-nitropyrazole (5.0 g, 19.6 mmol) in methanol (50 ml) was treated with silver nitrate (5.75 g, 33.8 mmol) and the mixture heated under reflux for 2 hours. The cooled reaction mixture was filtered and the filtrate evaporated under vacuum. The residue was partitioned between ethyl acetate (100 ml) and water (50 ml) and the aqueous phase extracted with a further quantity of ethyl acetate (50 ml). The organic extracts were combined, dried (MgSO4) and evaporated under vacuum. Chromatography on silica gel, eluting with a 97:3 mixture of dichloromethane and methanol, gave the title pyrazole as a white solid (1.6 g, 40%), m.p. 59°-63° C. Found: C,34.65; H,3.83; N,20.05. C6H8ClN3O3 requires C,35.05; H,3.92; N,20.44%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05346901 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-d60b8a033a6b45f4b6712072818c0bf3 |
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| Source note | uspto-grants-1994_09 |
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