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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28316Generated: October 26, 2026

Triphenylphosphine → 4-(4-Acryloyloxybutyloxy)-3-methyl-4'-phenylazo-azobenzene

https://huagongshe.com/reaction/28316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDisperse Yellow 7HCID 22736—
Reactant4-Hydroxybutyl acrylateHCID 75588—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Acryloyloxybutyloxy)-3-methyl-4'-phenylazo-azobenzeneHCID 17838592—

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 0.63 g of 4-hydroxy-3-methyl4′-phenylazo-azobenzene, 1.05 g of triphenylphosphine and 0.58 g of 4-hydroxybutylacrylate in 10 ml THF; which was cooled to −30° C., was added dropwise a solution of 0.70 g of diethyl azodicarboxylate in 5 ml THF. After complete addition, the reaction mixture was stirred for further 45 min at room temperature, and then concentrated to dryness. The obtained yellow-red residue was purified by filtration on silica using methylenechloride as the eluent to give 0.65 g of pure yellow-orange crystalys; λmax. (CB 483): 395 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419620B2
Source datasetuspto-grants-2008_09
ORD IDord-7b03299eb0ab4ce5adf307e56e52b766
Source noteuspto-grants-2008_09