HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418929Generated: October 25, 2026
3,6-Dimethoxypyridazine → HCID 44239664, compound
https://huagongshe.com/reaction/2418929
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,6-Dimethoxypyridazine | HCID 78348 | — |
| Reactant | 3-Iodooxetane | HCID 13356686 | — |
| Reagent | Hydrogen Peroxide | HCID 784 | — |
| Reagent | Sulfuric Acid | HCID 1118 | — |
| Catalyst | CID 516917 | HCID 516917 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 44239664 | HCID 44239664 | 22% |
Reaction Steps
H2O2 (30% in H2O; 0.23 mL, 2.25 mmol) was added dropwise over 5 min to a stirred solution of 3,6-dimethoxypyridazine 1e (100 mg, 0.75 mmol), concentrated H2SO4 (80 μL, 1.5 mmol), 3-iodooxetane (276 mg, 1.5 mmol) and iron(II) sulfate heptahydrate (63 mg, 0.225 mmol) in DMSO (7.5 mL) at 60 °C. After 1-2 min a further portion of iron(II) sulfate heptahydrate (50 mg, 0.19 mmol) was added and the mixture was stirred at 60 °C for 60 min. Ater allowing to cool, the mixture was poured into a 0.1 M solution of NaOH (30 mL) and EtOAc (30 mL). The aqueous and organic layers were partitioned and the aqueous layer was extracted with EtOAc (1 x 30 mL). The combined organic extracts were dried (Na2SO4), filtered and the solvent removed under vacuum to leave a crude oil. The oil was purified by column chromatography on silica gel to give the desired product 2e (33 mg, 22%) as a solid
Provenance & Evidence
| DOI | 10.1021/jo9010624 |
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| Source dataset | Minisci dataset from Roche |
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| ORD ID | ord-a3a62c7a1bce45b2814d4ba02fbb278b |
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| Source note | Minisci dataset from Roche |
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