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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79972Generated: October 26, 2026

Hexane → 2,6-Bis(tri-n-butylstannyl)-benzo[1,2-b:4,5-b']dithiophene

https://huagongshe.com/reaction/79972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantTributyltin ChlorideHCID 15096—
ReactantBenzo[1,2-b:4,5-b']dithiopheneHCID 11106168—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2,6-Bis(tri-n-butylstannyl)-benzo[1,2-b:4,5-b']dithiopheneHCID 5854558242%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of benzo[1,2-b:4,5-b′]dithiophene (820 mg, 4.3 mmol) in THF (100 mL) under argon at −78° C. was added a solution of n-butyllithium (2.5 M, 3.44 mL, 8.6 mmol). The solution was stirred at −78° C. for 30 minutes and then warmed to −20° C. for 30 minutes. Tri-n-butyltin chloride (2.34 mL, 8.6 mmol) was added and the reaction mixture was stirred at −20° C. for 30 minutes and then allowed to warm to room temperature. After 16 hours, hexane was added and the reaction was successively washed with water and brine, dried (MgSO4), concentrated and purified by flash chromatography (100% hexanes). 2,6-bis(tri-n-butylstannyl)-benzo[1,2-b:4,5-b′]dithiophene (1.4 g, 42%) was isolated along with product contaminated with the monostannylated benzodithiophene. 1H-NMR: 400 MHz, (CDCl3) δ: 8.27 (s, 2H), 7.38 (s, 2H), 1.65-1.57 (m, 12H), 1.41-1.32 (m, 12H), 1.26-1.11 (m, 12H), 0.91 (t, J=7.3 Hz, 18H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841278B2
Source datasetuspto-grants-2014_09
ORD IDord-f4bb72d0c4af46c5a6604ce826a41e6d
Source noteuspto-grants-2014_09