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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175101Generated: October 25, 2026

1-Decyne → 3-Decanyl-6-dec-1-ynyldithieno[3,2-b:2',3'-d]thiophene

https://huagongshe.com/reaction/1175101

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-DecyneHCID 12997—
Reactant2-Bromo-3-decanyldithieno[3,2-b:2',3'-d]thiopheneHCID 16103475—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventTriethylamineHCID 8471—
Product3-Decanyl-6-dec-1-ynyldithieno[3,2-b:2',3'-d]thiopheneHCID 6692501593%

Reaction Conditions

Temperature130 °C

Reaction Steps

2-bromo-3-decanyldithieno[3,2-b:2′,3′-d]thiophene (92)(4.16 g, 0.01 mol) was mixed with 1-decyne (3.6 g, 0.026 mol), tetrakis(triphenylphosphine)palladium (0.58 g, 0.5 mmol) and copper(I) iodide (0.19 g, 1.0 mmol) in triethylamine (80 mL). This mixture was bubbled with nitrogen for 5 minutes and then heated up to 130° C. under argon for 16 hours. Triethylamine was evaporated and hexane (150 mL) was added. This mixture was filtered to remove solid salts. The organic layer was washed with 1 M hydrochloric acid (50 mL) and brine (50 mL) then dried over MgSO4. The solvent was removed in vacuo, and the residue was purified by chromatography on silica gel eluting with hexane to yield the target compound (3.87 g, 93.0%). 1H NMR, solvent CD2Cl2. δ 7.36 (d, 1H), 7.30 (d, 1H), 2.82 (t, 2H), 2.49 (t, 2H), 1.63-1.27 (m, 28H), 0.88 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838623B2
Source datasetuspto-grants-2010_11
ORD IDord-19d7fa4606f246688414790cf03f8782
Source noteuspto-grants-2010_11