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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500791Generated: November 1, 2026

Tributyltin Chloride → 7-Chloro-2-(tributylstannyl)thieno[3,2-b]pyridine

https://huagongshe.com/reaction/500791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant7-Chlorothieno[3,2-b]pyridineHCID 11275251—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product7-Chloro-2-(tributylstannyl)thieno[3,2-b]pyridineHCID 5751665877%

Reaction Steps

To a solution of the chloride 2 (18.72 g, 110 mmol) in THF (200 mL) at −78° C. n-BuLi (51 mL, 127 mmol) was added and the reaction mixture was stirred for about 30 minutes. The tributylchlorostannane (25.4 mL, 93 mmol) was added and the mixture was stirred at −78° C. for another 60 minutes, quenched with water [at the same temperature] and allowed to warm up to room temperature. The warmed mixture was extracted with EtOAc, the extract was dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography, eluents EtOAc-hexane (15:85), then EtOAc-hexane (25:75) to afford title compound 98 (30.2 g, 77% yield) as a yellow oil. LRMS (M+1) 459.1 (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772247B2
Source datasetuspto-grants-2010_08
ORD IDord-d5857ef169e64a0480bf288fb131d880
Source noteuspto-grants-2010_08