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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635133Generated: October 26, 2026

Triphenylphosphine → 1-(4-[(E)-hex-2-enyloxy]phenyl)-4-pentylbicyclo[2.2.2]octane

https://huagongshe.com/reaction/635133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Hexen-1-olHCID 5318042—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantPhenol, 4-(4-pentylbicyclo[2.2.2]oct-1-yl)-HCID 21257800—
SolventTetrahydrofuranHCID 8028—
Product1-(4-[(E)-hex-2-enyloxy]phenyl)-4-pentylbicyclo[2.2.2]octaneHCID 21257791—

Reaction Steps

Triphenylphosphine (0.34 g, 0.0013 mol) was added in small portions to a solution of (E)-hex-2-en-1-ol (0.13 g, 0.0013 mol), 4-(4-pentylbicyclo[2.2.2]octyl)phenol (0.35 g, 0.0013 mol), diethylazodicarboxylate (0.22 g, 0.0013 mol) in dry tetrahydrofuran (20 cm3), cooled in an ice bath under an atmosphere of nitrogen. The reaction mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure and the crude product was purified by column chromatography on silica gel using a 9:1 petroleum ether (40-60° C./ethyl acetate mixture as eluent, followed by recrystallisation from ethanol to yield 0.18 g (39%), K 69° C., SA-N 59° C., N-I 134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06187393B1
Source datasetuspto-grants-2001_02
ORD IDord-20aad75121be4c4ab75a9846bc46596a
Source noteuspto-grants-2001_02