HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → 4-Methanesulphinyl-3-nitrobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | 4-Methanesulphinyl-3-nitrobenzoic acid 4-Methylthio-3-nitrobenzoic acid | HCID 86756413 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Methanesulphinyl-3-nitrobenzoic acid | HCID 22168648 | 181.5% |
Reaction Steps
The starting materials were prepared as follows: 4-Methanesulphinyl-3-nitrobenzoic acid 4-Methylthio-3-nitrobenzoic acid (4.36 g, 20 mM) was dissolved in acetic acid (200 ml), and treated at ambient temperature with H2O2 (2.5 ml, 30%, 22 mN). After stirring at ambient temperature for 4 days, excess peroxide was decomposed with sodium metabisulfite, and solvent evaporated. The residue was purified by chromatography on silica, eluting with methanol, to give 4-methanesulphinyl-3-nitrobenzoic acid (4.1 g, 89%), mp 238-2390. Nmr (DMSO-d6): δ 2.90 (s, 3H); 8.29 (d, 1H); 8.56 (dd, 1H); 8.68 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06187804B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-5410e222e9284c0ead1a5a73df0a1aec |
| Source note | uspto-grants-2001_02 |