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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716981Generated: November 2, 2026

Hexane → Stannane, [2,2'-bithiophen]-5-yltrimethyl-

https://huagongshe.com/reaction/1716981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantTrimethyltin chlorideHCID 14016—
Reactant2,2'-BithiopheneHCID 68120—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductStannane, [2,2'-bithiophen]-5-yltrimethyl-HCID 1103484664%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 3-necked flask equipped with a glass stopper, rubber septum and a nitrogen inlet was added 2,2′-bithiophene (10 g, 60.1 mmol) and anhydrous THF (100 mL). The dark (green) solution was cooled to 0° C. A 2.5 M solution of n-BuLi in hexane (26.4 mL, 66 mmol) was added via syringe. The reaction mixture was then stirred at 25° C. for 1.5 hours. The mixture was cooled to −78° C. and a 1.0 M solution of trimethylstannyl chloride in THF (66 mL, 66 mmol) was added slowly via syringe. The reaction mixture was allowed to warm to 25° C. and was stirred overnight. THF was removed in vacuo and the residue was dissolved in pentane (200 mL). The pentane layer was washed with water (3×200 mL), dried over MgSO4, and the pentane was removed in vacuo to yield a green oil. The oil was purified by vacuum distillation (118-120° C., 0.6 mmHg) to yield 12.5 g (64%) of product MS=330.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803885B2
Source datasetuspto-grants-2010_09
ORD IDord-432b9a573a294b69a32f61bf78aea977
Source noteuspto-grants-2010_09