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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278505Generated: November 1, 2026

2-(Tri-n-butylstannyl)thiophene → HCID 22996756, compound

https://huagongshe.com/reaction/278505

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tri-n-butylstannyl)thiopheneHCID 2779373—
Reactant2,6-Dibromo-1,4,5,8-tetramethoxynaphthaleneHCID 14360314—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 22996756HCID 2299675696%

Reaction Steps

1,4,5,8-Tetramethoxy-2,6-dibromonaphthalene (7.80 g., 0.019 mol.) and 2-(tributylstannyl)thiophene (18.00 g., 0.048 mol.) were dissolved in 200 mL dry toluene under argon atmosphere. Pd(PPh3)4 (100 mg.) was introduced into the reaction flask using a Schlenk tube under argon. The resultant mixture was subsequently refluxed for 18 hrs. The brownish black solution was cooled and poured into 500 mL of petroleum ether to afford crude yellow solid. Upon recrystallization from CH2Cl2/petroleum ether (1:3) the desired product was obtained as a light yellow solid. Yield: 96%. M. p. 233.5-237° C. Anal. Calcd. for C22H20O4S2: C, 64.06%; H, 4.89%; S, 15.54%. Found: C, 64.12%; H, 4.90%; S, 15.12%. Mass spectrum: 411.84 (M+). 1H-NMR (CDCl3; in ppm.): 3.73 (s, 3H), 4.05 (s, 3H), 7.13 (dd, 2H), 7.19 (s, 2H), 7.41 (dd, 2H), 7.59 (dd, 2H,). 13C-NMR (CDCl3; in ppm.): 56.7, 61.7, 107.5, 122.5, 124.4, 125.7, 126.6, 126.9, 139.1, 146.5, 152.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06359149B1
Source datasetuspto-grants-2002_03
ORD IDord-c040752292384a96af82492762bdb848
Source noteuspto-grants-2002_03