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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589190Generated: October 31, 2026

Tributyltin Chloride → 2-((Tert-butyldimethylsilyloxy)methyl)-5-(tributylstannyl)thiazole

https://huagongshe.com/reaction/589190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-((Tert-butyldimethylsilyloxy)methyl)thiazoleHCID 21480592—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product2-((Tert-butyldimethylsilyloxy)methyl)-5-(tributylstannyl)thiazoleHCID 6729435277.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-((tert-butyldimethylsilyloxy)methyl)thiazole (8.0 g, 35 mmol) was dissolved in dry THF (350 mL) and the solution was cooled to −78° C. To this solution, t-BuLi (1.7 M, 25 mL, 42 mmol) was added dropwise. The reaction was warmed to −40° C. and stirred for 2 hours. Then, Bu3SnCl (14.6 g, 45 mmol) was added and the resulting mixture was allowed to warm to room temperature slowly and stirred for another 30 min. NH4Cl (aq.) was added to quench the reaction and extracted with EtOAc. The organics was dried and concentrated. The residue was purified with column (silica gel, 0˜30 EtOAc/hexane) to give the product 2-((tert-butyldimethylsilyloxy)methyl)-5-(tributylstannyl)thiazole (14.1 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227971B2
Source datasetuspto-grants-2016_01
ORD IDord-481e3b87cacc44ddbbcc93050697583b
Source noteuspto-grants-2016_01