Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | 2-Chloro-4-methylpyridine | HCID 77248 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 18518311 | HCID 18518311 | 101.6% |
Reaction Steps
A mixture of 2-chloro-4-methylpyridine (10.0 g, 78.3 mmole) and 34% peracetic acid (76.05 g, 91.0 mmole) in glacial AcOH (10 mL) was heated at 70° C. for 3 hr. The reaction mixture was cooled, conc. HCl (35 mL) was added, and the mixture was concentrated on the rotavap. Recrystallization from n-butanol followed by trituration with ether gave the title compound (7.16 g, 51%) as a white solid: MS (ES) m/e 143.9 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06576643B2 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-952c70811f4447e38fbd608ad28449a5 |
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| Source note | uspto-grants-2003_06 |
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