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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-Butyn-2-olHCID 16239—
Reactant2-Bromo-6-decyloxynaphthaleneHCID 613821—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventDiethylamineHCID 8021—
Product(+)-6-Decyloxy-2-(3-hydroxy-1-butynyl)naphthaleneHCID 1943753881%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534188
Source datasetuspto-grants-1996_07
ORD IDord-5a22831c6a0a403a84c01872963ac725
Source noteuspto-grants-1996_07