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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291589Generated: October 30, 2026

2,2'-Bithiophene → (2,2':5',2''-Terthiophene)-5-carboxaldehyde

https://huagongshe.com/reaction/1291589

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2'-BithiopheneHCID 68120—
Reactant2-Thiophenecarboxaldehyde, 5-iodo-HCID 3014361—
CatalystMercuryHCID 23931—
SolventAcetonitrileHCID 6342—
Product(2,2':5',2''-Terthiophene)-5-carboxaldehydeHCID 454742—

Reaction Steps

1 g of 5-iodo-2-thiophenecarboxaldehyde was dissolved in 200 ml of acetonitrile. 0.7 g of bithiophene was added into the solution under nitrogen gas atmosphere for 1 hour and irradiated under 100 W mercury-vapor lamp light for 12 hours. The solution was monitored by thin layer chromatography. At this stage, about 60% product was generated. The acetonitrile was removed from the reaction solution under reduced pressure and CH2Cl2 was added for extraction. After the extract was filtered through silica gel layer and separated by column chromatography, starting material was recovered from the eluate of ethyl acetate/n-hexane 1/9 fraction and 5-formyl-2,2':5',2"-terthiophene was obtained from the eluate of ethyl acetate/n-hexane 3/7 fraction respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753692
Source datasetuspto-grants-1998_05
ORD IDord-2427d5ef74a3430d87bf5240c1113068
Source noteuspto-grants-1998_05