HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927077Generated: October 26, 2026
1-Chloro-3-iodobenzene → 3,4-Bis(benzyloxy)-6-((3-chlorophenyl)ethynyl)pyridazine
https://huagongshe.com/reaction/927077
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-3-iodobenzene | HCID 12269 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 3,4-Bis(benzyloxy)-6-ethynylpyridazine | HCID 86677025 | — |
| Reactant | 1,8-Diazabicycloundec-7ene | HCID 129662960 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,4-Bis(benzyloxy)-6-((3-chlorophenyl)ethynyl)pyridazine | HCID 71269950 | 30% |
Reaction Steps
To a solution of 1-chloro-3-iodobenzene (0.862 g, 3.62 mmol) in dry tetrahydrofuran (11 ml) was added copper(I) iodide (0.063 g, 0.33 mmol), bis(triphenylphosphine)-palladium(II) chloride (0.115 g, 0.16 mmol) and 1,8-diazabicycloundec-7-ene and (DBU; 2.97 ml, 19.72 mmol). The reaction was then purged and evacuated with nitrogen several times before 3,4-bis(benzyloxy)-6-ethynylpyridazine (Intermediate 5; 1.04 g, 3.29 mmol) was added. The reaction vessel was sealed and heated to 80° C. for 1 hour. Upon cooling, the resultant mixture was partitioned between ethyl acetate and water. The combined organic portions were washed with water (×2) and brine, dried (MgSO4), filtered and concentrated to give a brown oil. The crude oil was purified by silica chromatography (eluting with 0-20% ethyl acetate in petrol) to yield 3,4-bis(benzyloxy)-6-((3-chlorophenyl)ethynyl)pyridazine as a yellow solid (yield=30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290456B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-38160e5aef3340c1881c66303169bfe1 |
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| Source note | uspto-grants-2016_03 |
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