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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646539Generated: October 29, 2026

Carbon Dioxide → 3,6-Dihexylthieno[3,2-b]thiophene

https://huagongshe.com/reaction/646539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantQuinolineHCID 7047—
Reactant3,6-Dihexylthieno[3,2-b]thiophene-2-carboxylic acidHCID 16103485—
CatalystCopperHCID 23978—
SolventHexaneHCID 8058—
Product3,6-Dihexylthieno[3,2-b]thiopheneHCID 1610345568.6%

Reaction Conditions

Temperature262 °C

Reaction Steps

A mixture of compound 55 (30 g, 0.085 mol), copper powder (3.76 g) and quinoline (80 mL) was heated at 264-260° C. in a Woods metal bath. When no further bubbles of carbon dioxide gas could be detected (about 2 hours), the mixture was allowed to cool to room temperature and hexane (200 mL) was added. This mixture was washed repeatedly with HCl (1-2 M in water) to remove the quinoline. The remaining organic layer was dried over MgSO4 and concentrated by evaporation, leaving a residue, which was purified by column chromatography (SiO2/hexanes) to yield compound 57 (18 g, 68.4%). m.p. 57.5-59.1° C., 1H NMR (CD2Cl2): δ 6.97 (s, 2H), 2.70 (t, 4H), 1.73 (m, 4H), 1.37 (m, 12H), 0.88 (t, 6H). 13C NMR: 136.56, 134.96, 109.80, 31.94, 29.31, 29.28, 28.47, 22.96, 14.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705108B2
Source datasetuspto-grants-2010_04
ORD IDord-094d31f516ac4403ba1ffde2bebe3bc5
Source noteuspto-grants-2010_04