HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230132Generated: October 30, 2026
2-Methylpyridine → HCID 59834315, compound
https://huagongshe.com/reaction/230132
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylpyridine | HCID 7975 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178503459 | HCID 178503459 | — |
| Product | HCID 59834315 | HCID 59834315 | — |
Reaction Steps
To a cooled (ice bath) mixture of (2-chlorophenyl)-(4-hydroxy-2-methylsulfanylpyrimidin-5-yl)methanone (18.72 g, 66 mmol) and picoline (3.95 mL, 39.6 mmol) was added dropwise phosphoryl chloride (37.3 mL, 396 mmol) via an addition funnel. The resulting mixture was removed from the ice bath and heated to 80° C. for 2 hours. The reaction was cooled to ambient temperature and poured onto ice (250 mL). Ethyl acetate was added and the layers were partitioned and separated. The organic layer was further washed with two consecutive solutions of saturated sodium bicarbonate (150 mL) followed by brine (150 mL). The aqueous layers were back extracted with ethyl acetate (2×150 mL). The combined ethyl acetate layers were dried over magnesium sulfate, filtered and concentrated to give the product as a yellow solid (17.36 g, (M+H)+=299.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07566708B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-82249a4211df4472a2bfc19c5b53edc3 |
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| Source note | uspto-grants-2009_07 |
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