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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121309Generated: October 26, 2026

Triphenylphosphine → 2-[(E)-hex-2-enyloxy]-5-(4'-hexylbiphenyl-4-yl)thiophene

https://huagongshe.com/reaction/2121309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Hexen-1-olHCID 5318042—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant2-Hydroxy-5-(4'-hexylbiphenyl-4-yl)thiopheneHCID 23432173—
SolventTetrahydrofuranHCID 8028—
Product2-[(E)-hex-2-enyloxy]-5-(4'-hexylbiphenyl-4-yl)thiopheneHCID 2343218119.3%

Reaction Steps

Triphenylphosphine (1.4 g) is added in small portions to a solution of (E)-hex-2-en-1-ol (0.60 g), 2-hydroxy-5-(4′-hexylbiphenyl-4-yl)thiophene (0.50 g), diethylazodicarboxylate (0.80 g) in dry tetrahydrofuran (100 cm3) at 0° C. under an atmosphere of nitrogen. The reaction mixture is stirred at room temperature overnight. The solvent is removed under reduced pressure and the crude product was purified by column chromatography on silica gel using a 4:1 petroleum (40-60° C.) ether/ethyl acetate mixture as eluent, followed by recrystallisation from ethanol to yield 0.12 g of 2-[(E)-hex-2-enyloxy]-5-(4′-hexylbiphenyl-4-yl)thiophene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696110B1
Source datasetuspto-grants-2004_02
ORD IDord-31d202eed6e74b5e96675609941c9056
Source noteuspto-grants-2004_02