Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596693Generated: November 1, 2026

2-(Tri-n-butylstannyl)thiophene → HCID 22996753, compound

https://huagongshe.com/reaction/1596693

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tri-n-butylstannyl)thiopheneHCID 2779373—
ReactantNaphthalene, 1,5-dibromo-4,8-dimethoxy-HCID 11131763—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 22996753HCID 2299675381%

Reaction Steps

1,5-Dimethoxy-4,8-dibromonaphthalene (1.19 g., 0.0034 mol.) and 2-(tributylstannyl)thiophene (3.85 g., 0.0103 mol.) were dissolved in 100 mL dry toluene in 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 300 mL of petroleum ether to afford crude yellow solid. Upon recrystallization from CH2Cl2:petroleum ether (1:5), the desired product was obtained as a light yellow solid. Yield: 81%. M.p. 216-218° C. Anal. Calcd. for C20H16O2S2: C, 68.15%; H, 4.58%; S, 18.19%. Found: C, 67.64%; H, 4.48%; S, 17.49%. Mass spectrum: 351.75 (M+). 1H-NMR (CDCl3; in ppm): 3.59 (s, 3H), 6.81 (d, 2H), 6.89 (d, 2H), 7.00 (dd, 2H), 7.26 (dd, 2H), 7.38 (d, 2H). 13C-NMR CDCl3; in ppm): 55.6, 106.5, 123.1, 123.5, 125, 125.5, 126.1, 131.1, 147.5, 156.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291621B1
Source datasetuspto-grants-2001_09
ORD IDord-5d37f5b56c164840b655205f54d476a9
Source noteuspto-grants-2001_09