HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678397Generated: October 30, 2026
Phosphorus oxychloride → 3-Chloro-6-methyl-5-(4-methylphenyl)-4-(2,4,6-trifluorophenyl)pyridazine
https://huagongshe.com/reaction/1678397
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-methyl-5-(4-methylphenyl)-4-(2,4,6-trifluorophenyl)-2H-pyridazin-3-one | HCID 57793916 | — |
| Product | 3-Chloro-6-methyl-5-(4-methylphenyl)-4-(2,4,6-trifluorophenyl)pyridazine | HCID 25271420 | — |
Reaction Steps
19.77 g of 6-methyl-5-(4-methylphenyl)-4-(2,4,6-trifluorophenyl)-2H-pyridazin-3-one and 100 ml of phosphorus oxychloride were mixed and stirred at 110° C. for 1 hour. The reaction mixture was allowed to cool down to room temperature and concentrated under reduced pressure. To the residue was added chloroform and ice water, and was separated to two layer. The organic layer was washed sequentially with water and saturated brine, and dried over anhydrous sodium sulfate, then, concentrated under reduced pressure, to obtain 19.90 g of 3-chloro-6-methyl-5-(4-methylphenyl)-4-(2,4,6-trifluorophenyl)pyridazine (hereinafter, referred to as compound (xxii) of the present invention).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008512B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-4b57d23868d245fb980e1249ddbb086f |
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| Source note | uspto-grants-2011_08 |
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