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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581845Generated: October 31, 2026

1-Naphthaldehyde → HCID 12192538, compound

https://huagongshe.com/reaction/1581845

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphine OxideHCID 13097—
ReactantPhosphoniumHCID 5460504—
CatalystPhosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
SolventToluene hexaneHCID 21889329—
ProductHCID 12192538HCID 1219253863%

Reaction Steps

1-(ethyl)-2-(naphthyl)ethylene (IXd) was prepared from 1.00 g (2.7 mmol) of (ethyl)triphenylphosphonium bromide (Vd), 0.42 g (2.7 mmol) of naphthaldehyde and 0.79 g (5.5 mmol) of anhydrous K2CO3 by ball-milling for 26 hours. The formed powder was analyzed by the solid state 31P MAS NMR spectroscopy. The solid state 31P MAS NMR spectrum of the ball-milled powder contained two signals: a major signal corresponding to triphenylphosphine oxide at δ31P=25 ppm and a minor signal corresponding to the starting phosphonium salt at δ31P=30 ppm, the estimated ratio ˜8:1. The powder (2.0 g) was loaded on the top of a silica-gel filled chromatographic column, and the mixture of (E)- and (Z)-isomers was isolated by eluation with a hexane-toluene mixture (E:Z ratio ca. 1:1 by 1H NMR in CDCl3) in the 63% yield, (0.26 g). Triphenylphosphine oxide was further obtained from the same column in 80% yield (0.61 g) using a hexane-acetone mixture as an eluant. Assignment of the signals in the 13C and 1H NMR spectra of the reaction products was performed according to the literature (see, e.g., Kulasegarm, et al., J. Org. Chem. 62, 6547 (1997); Kulasegarm et al., Tetrahedron 54, 1361(1998)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730812B2
Source datasetuspto-grants-2004_05
ORD IDord-553bbe0382de4df7b9cb1a9a271d6afc
Source noteuspto-grants-2004_05