HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 10265074, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | (R)-alpha-hexyl-4-nitro-1H-imidazole-1-acetic acid | HCID 9881517 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10265074 | HCID 10265074 | 2,813.6% |
Reaction Steps
(R)-2-(4-Nitro-1H-imidazol-1-yl)-octanoic acid (16.0 g, 63.0 mmol) was dissolved in 1 L of anhydrous methanol. To this solution was added pTsOH (300 mg). The reaction was then heated to reflux for 16 hours. Upon cooling, the solvent was removed in vacuo, to give an oil that was dissoved in 300 mL of ethyl acetate. The solution was washed (2×250 mL) with saturated NaHCO3 solution. The organic was then dried (Na2SO4) and concentrated in vacuo to provide 13.2g (78%) of (R)-methyl-2-(4-nitro-1H-imidazol-1-yl)-octanoate as an amber oil. Calculated for C12H19N3O4 : C, 53.32; H, 7.11; N, 15.60. Found: C, 53.23; H, 7.05; N, 15.39.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05484780 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-cca8a2ea75ba4981ac658cdcaf9840c4 |
| Source note | uspto-grants-1996_01 |