Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 16752340 | HCID 16752340 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21915845 | HCID 21915845 | — |
Reaction Steps
3.33 g (0.01289 mol) of [1,1′;3′,1″]terphenyl-5′-carbaldehyde are dissolved in 12 ml of THF and added to methyltriphenylphosphonium bromide solution. The yellowish mixture is stirred at 0° C. for 1 h. After cooling to room temperature, the mixture is taken up in dichloromethane. The solution is washed with water, and the combined organic phases are dried over sodium sulfate. The mixture is evaporated to dryness. Column chromatography is carried out with hexane/ethyl acetate. The column chromatography results in a yield of 2.4 g (71%) of clean substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08786181B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-1ca1f472406441cdb24fcfa57bafc9e6 |
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| Source note | uspto-grants-2014_07 |
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