Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl nitrite | HCID 12231 | — |
| Reactant | HCID 11726686 | HCID 11726686 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 73081857 | HCID 73081857 | 91.3% |
Reaction Steps
Methyl nitrite [prepared from sodium nitrite (1.4 g), methanol (0.9 ml) and sulfuric acid (0.7 ml) in water (2.3 ml)] was introduced into an ice-cooled mixture of 2'-(2,4-difluorophenylthio)-4'-propionylmethanesulfonanilide (2.54 g) in tetrahydrofuran (10 ml) and 12% hydrogen chloride in ether (10 ml). The mixture was stirred for 5 hours at 3° C. and evaporated. The residual solid was recrystallized from ethanol to give colorless crystals of 2'-(2,4-difluorophenylthio)-4'[2-(hydroxyimino)-1-oxopropyl]methanesulfonanilide (2.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05034417 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-78170ce767174f60989fe7573789dd3b |
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| Source note | uspto-grants-1991_07 |
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