HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193241Generated: October 31, 2026
Ytterbium triflate → HCID 66823720, compound
https://huagongshe.com/reaction/1193241
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ytterbium triflate | HCID 2733225 | — |
| Reactant | Lithium perchlorate | HCID 23665649 | — |
| Reactant | HCID 86663673 | HCID 86663673 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 66823720 | HCID 66823720 | 15.8% |
Reaction Steps
To a mixture of 2-(2′,4′-dichloro-4-cyclopropylbiphenyl-3-yl)-4,4,6,6-tetramethyl-1,5-dioxa-spiro[2.4]heptan-7-one (17.80 g, 0.041 mol) and ytterbium triflate (2.20 g, 4.41 mmol) is added a solution of 5M lithium perchlorate (prepared from 42 ml diethyl ether and 22.30 g lithium perchlorate). The resulting suspension is stirred at room temperature for 17 days, at which stage further diethyl ether (42 ml), lithium perchlorate (22.3 g, 0.21 mol) and ytterbium triflate (19.8 g, 0.035 mol) is added. The reaction mixture is then heated at 27° C. (internal temperature) for 1 day, followed by partitioning between diethyl ether and distilled water. The two phases are separated, the aqueous phase is extracted with diethyl ether (×2), and then all organic fractions are combined, washed with brine then dried over magnesium sulphate. The suspension is filtered and the filtrate is concentrated in vacuo. The crude material is purified by flash column chromatography (ethyl acetate/hexane eluant) to give an oil which is triturated with hexanes to afford 4-(2′,4′-dichloro-4-cyclopropylbiphenyl-3-yl)-2,2,6,6-tetramethylpyran-3,5-dione (2.80 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680299B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-13a11c9570a04173b9b11f07a2eabb4e |
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| Source note | uspto-grants-2014_03 |
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