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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220121Generated: October 29, 2026

Benzothiazole → 2-(Tributylstannyl)-1,3-benzothiazole

https://huagongshe.com/reaction/2220121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzothiazoleHCID 7222—
ReactantTributyltin ChlorideHCID 15096—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product2-(Tributylstannyl)-1,3-benzothiazoleHCID 3762392—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyllithium (1.6M, 10 mL, 15.98 mmol) was added to a solution of benzothiazole (1.80 g, 13.3 mmol) in anhydrous ether (30 ml) stirred at −78° C. under nitrogen. After 10 min, tri-n-butylstannyl chloride (4.33 g, 13.31 mmol) was added, then the solution 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, filtered, and evaporated to give the sub-title compound as a brown oily residue (5.0 g), which was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417050B2
Source datasetuspto-grants-2008_08
ORD IDord-9890acb71d2f4827bd88e2b812d65f4c
Source noteuspto-grants-2008_08