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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121303Generated: October 27, 2026

Triphenylphosphine → 2-(4-[(e)-Hex-2-enyloxy]phenyl)-5-octylthiazole

https://huagongshe.com/reaction/2121303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Hexen-1-olHCID 5318042—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant2-(4-Hydroxyphenyl)-5-octylthiazoleHCID 135844842—
SolventTetrahydrofuranHCID 8028—
Product2-(4-[(e)-Hex-2-enyloxy]phenyl)-5-octylthiazoleHCID 23432086—

Reaction Steps

Triphenylphosphine (0.95 g) is added in small portions to a solution of (E)-hex-2-en-1-ol (0.40 g), 2-(4-hydroxyphenyl)-5-octylthiazole (0.70 g), diethylazodicarboxylate (0.60 g) in dry tetrahydrofuran (40 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 0.15 g of 2-(4-[(E)-hex-2-enyloxy]phenyl)-5-octyfthiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696110B1
Source datasetuspto-grants-2004_02
ORD IDord-a097de3f9d71474190a55feb879d52ec
Source noteuspto-grants-2004_02