HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615722Generated: October 30, 2026
2,2'-Bipyridine → HCID 20427189, compound
https://huagongshe.com/reaction/615722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2'-Bipyridine | HCID 1474 | — |
| Reactant | 1,3-Cyclopentanedione | HCID 77466 | — |
| Reactant | HCID 20427191 | HCID 20427191 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 20427189 | HCID 20427189 | — |
Reaction Steps
To THF (250 ml) under N2 with stirring is added cyclopentane-1,3-dione (0.10 mol) and 2,2'-bipyridyl (~3-5 mg) as an indicator. After cooling to -70°, n-butyllithium in hexane is added slowly while the temperature is allowed to rise to -5° near the end of the addition (~130 ml of 1.6M solution, 0.20 mol). After the pink indicator persists at -5°, the mixture is recooled to -65° and 4-(4-trifluoromethylphenoxy)phenoxyacetyl chloride is added dropwise over 5 min. After 1 hour, the reaction mixture diluted with water & ether is added. The organic layer is is washed with water, dried over sodium sulfate and concentrated in vacuo to give 2-[4-(4-trifluoromethylphenoxy)phenoxyacetyl]cyclopentane-1,3-dione (V; Y is H, Z is CF3, R1 is H and n is one).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04500737 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-de99f480f94a42b9a7d34180d4efc138 |
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| Source note | uspto-grants-1985_02 |
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