HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734395Generated: October 26, 2026
Triphenylphosphine → (+)-6-Decyloxy-2-(3-hydroxy-1-butynyl)naphthalene
https://huagongshe.com/reaction/1734395
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Butyn-2-ol | HCID 16239 | — |
| Reactant | 2-Bromo-6-decyloxynaphthalene | HCID 613821 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Diethylamine | HCID 8021 | — |
| Product | (+)-6-Decyloxy-2-(3-hydroxy-1-butynyl)naphthalene | HCID 19437538 | 81% |
Reaction Steps
18.2 g (0.05 mol) of 6-decyloxy-2-bromonaphthalene (VI-59), 10.5 g (0.15 mol) of (+)-3-butyn-2-ol (VII*-59), 0.4 g of copper iodide, 0.7 g of triphenylphosphine, 0.4 g of bis(triphenylphosphine)palladium chloride and 100 ml of diethylamine were stirred under reflux for 12 hours in an atmosphere of nitrogen gas. After completion of the reaction, the reaction mixture was poured into ice/aqueous hydrochloric acid and extracted with 200 ml of ethyl acetate. The organic layer was further washed with water and concentrated under reduced pressure. The residue was purified by silica gel chromatography using toluene-ethyl acetate as eluent to obtain 14.3 g (yield 81%) of optically active (+)-6-decyloxy-2-(3-hydroxy-1-butynyl)naphthalene (I'-59), mp 74°-75° C. [α]D20 =+16.9° (c=1, chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05534188 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-5a22831c6a0a403a84c01872963ac725 |
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| Source note | uspto-grants-1996_07 |
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