HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424315Generated: October 31, 2026
Phosphorus oxychloride → HCID 57457877, compound
https://huagongshe.com/reaction/2424315
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 22940221 | HCID 22940221 | — |
| Reactant | HCID 23013839 | HCID 23013839 | — |
| Product | HCID 57457877 | HCID 57457877 | — |
Reaction Steps
0.02 mL (0.22 mmol) of phosphorus oxychloride was added to 27.6 mg (0.0949 mmol) of a mixture of 6-chloro-3-(2,3,5-trimethyl-6-vinylphenoxy)pyridazine 1-oxide and 3-chloro-6-(2,3,5-trimethyl-6-vinylphenoxy)pyridazine 1-oxide obtained in (6), and the resulting mixture was stirred at room temperature for 2 hours. To the mixture was added 0.4 mL of chloroform, and the resulting mixture was stirred at room temperature overnight. The reaction mixture was concentrated, 0.2 mL (2.2 mmol) of phosphorus oxychloride was added to the residue and the resulting mixture was stirred at room temperature for 5 hours. The reaction mixture was concentrated, the residue was purified by preparative thin-layer chromatography (available from MERCK CO., 1.05744, 1 plate was used, developed by hexane:ethyl acetate=5:1) to obtain 5.0 mg (0.016 mmol, Yield: 17%) of 4,6-dichloro-3-(2,3,5-trimethyl-6-vinylphenoxy)pyridazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964531B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-a61cc470678d4302bdb3cfdb03c80e25 |
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| Source note | uspto-grants-2011_06 |
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