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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 439657Erstellt: 24. Oktober 2026

Thiophene-2,5-dicarbaldehyde → 3-Dodecylthiophene

https://huagongshe.com/de/reaction/439657

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiophene-2,5-dicarbaldehydeHCID 587784—
Edukt2,2'-(Thiophene-2,5-diyl)diacetonitrileHCID 12119796—
Produkt3-DodecylthiopheneHCID 2733655—

Reaktionsschritte

Heterocycles can also be easily included in the copolymer chain. The literature records the preparation of an insoluble cyano-substituted alternating polymer derived from thiophene-2,5-diacetonitrile and thiophene-2,5-dicarboxaldehyde (Kossmehl, G. Ber. Bunsenges. Phys. Chem., 1979, 83, 417) and copolymers based on the thiophene-2,5-dicarboxaldehyde and 2,5-dimethoxyterephthaldehyde (H. Horhold, Z. Chem., 1972, 12). The bischloromethylation of 3-dodecylthiophene gave the unstable product (17), which was immediately treated with cyanide to give the bisnitrile (18). Alternatively, the bis-aldehyde (19) can be synthesized from (17) in 3 steps in an analogous fashion to before. Condensation of (18) with (7) gave a purple polymer (onset of absorbance of 670 nm).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05514878
Quelldatensatzuspto-grants-1996_05
ORD IDord-8dee216498d54aae9cbbe9c167ce86e1
Quellennotizuspto-grants-1996_05