Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Tetrahydro-2-hydroxyfuran | HCID 93002 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Benzyltriphenylphosphonium chloride | HCID 70671 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Phenylpent-4-enyl-1-ol | HCID 5371695 | — |
Reaction Steps
To a suspension of 4 g of benzyltriphenylphosphonium chloride in 20 ml of tetrahydrofuran was added 7.07 ml of 1.6M hexane solution of n-butyl lithium under cooling at 0° C. After stirring at room temperature for 30 minutes, 1 g of 2-hydroxytetrahydrofuran was added, followed by stirring at room temperature for 16 hours. Subsequently, after refluxing for 2 hours, insolubles were filtered off and the solvent was distilled off. The residue was purified by silica gel column chromatography (solvent: hexane-ethyl acetate=2:1) to give 2 g of (E)-5-phenyl-4-penten-1-ol as a colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04886817 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-021a769ec5bf44a297e6ddea2e4655b7 |
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| Source note | uspto-grants-1989_12 |
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