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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220124Generated: October 30, 2026

Benzoxazole → 2-Triethylstannylbenzoxazole

https://huagongshe.com/reaction/2220124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoxazoleHCID 9228—
ReactantTriethyltin bromideHCID 17701—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product2-TriethylstannylbenzoxazoleHCID 68978634—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyllithium (1.6M, 6.0 mL, 9.57 mmol) was added to a solution of benzoxazole (950 mg, 7.98 mmol) in anhydrous ether (20 mL) stirred at −78° C. under nitrogen. After 10 min, triethylstannyl bromide (2.28 g, 7.98 mmol) was added, then the reaction mixture was allowed to warm to room temperature, and stirred for another 1 h. The mixture was quenched, and washed with 1N sodium hydroxide, dried through MgSO4, and then the solvent was evaporated to give the sub-title compound as a brown oily residue which was used directly without further purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417050B2
Source datasetuspto-grants-2008_08
ORD IDord-a6ccd87adc674d4f91f8b3b25741e14f
Source noteuspto-grants-2008_08