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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596089Generated: October 29, 2026

Dimethylformamide → Terephthalaldehyde

https://huagongshe.com/reaction/1596089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriphenylphosphineHCID 11776—
Reactant1,4-Bis(bromomethyl)-2,5-bis(heptyloxy)benzeneHCID 18431915—
ProductTerephthalaldehydeHCID 12173—
ProductPhosphoniumHCID 5460504—

Reaction Steps

A phosphonium salt (A) was synthesized by the reaction of 2,5-diethyl-P-xylylene dibromide with triphenylphosphine in an N,N-dimethylformamide solvent, and a phosphonium salt (B) was synthesized by the reaction of 2,5-diheptyloxy-p-xylylene dibromide with triphenylphosphine in an N,N-dimethylformamide solvent. The obtained two phosphonium salts (A) (4.1 parts by weight) and (B) (1.0 part by weight) and terephthalaldehyde (0.8 parts by weight) were dissolved in ethyl alcohol. For a 3-hour polymerization, an ethyl alcohol solution containing 0.8 parts by weight of lithium ethoxide was added dropwise to an ethyl alcohol solution of the phosphonium salts and dialdehyde at room temperature. After allowed to stand alone at room temperature overnight, the precipitate was filtered out, washec. with ethyl alcohol, and dissolved in chloroform, to which ethanol was added for re-precipitation. The obtained product was dried under reduced pressure to obtain 0.35 parts by weight of the end polymer. This is called a polymeric fluorescent substance 1. Set out below are the repeating unit in polymeric fluorescent substance 1 and its molar ratio calculated from the charge ratio of monomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288487B1
Source datasetuspto-grants-2001_09
ORD IDord-dbdd038c87224f9cb8bb7c5658d722fa
Source noteuspto-grants-2001_09