HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265289Generated: October 29, 2026
Tributylphosphine → [2-(3-Butenyloxy)ethyl]benzene
https://huagongshe.com/reaction/265289
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 2-Nitrophenyl selenocyanate | HCID 103931 | — |
| Reactant | 4-Phenethoxybutan-1-ol | HCID 19082188 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(3-Butenyloxy)ethyl]benzene | HCID 12936829 | 92% |
Reaction Steps
To a solution of 4-[2-phenylethoxy]butanol (3.16 g) and 2-nitrophenyl selenocyanate (4.0 g) in THF (50 ml) under argon was added tributylphosphine (4.5 ml) in THF (2 ml) dropwise over 30 min. After a further 2 hours at room temperature the solvent was removed under reduced pressure. A further 50 ml of THF was added and the mixture cooled to 0° at which point H2O2 (17 ml, 30% aqueous v/v) was added to the stirred solution over 1 hour. The mixture was allowed to warm to room temperature and stirring continued overnight. The solvent was removed under reduced pressure and the residue taken up in ether, washed with 1 molar aqueous hydrochloric acid, sodium bicarbonate solution and brine. The solution was dried, filtered and the solvent removed under reduced pressure to yield a yellow oil which was purified by chromatography using diethyl ether in petroleum ether (bp 60°-80°) as eluant to yield the subtitled compound (2.63 g, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05648370 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-e16f9956e7f54821a41eb06781a97ec8 |
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| Source note | uspto-grants-1997_07 |
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