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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455648Generated: November 1, 2026

Acetone → 2-[5-(Tributylstannyl)-1,3-thiazol-2-yl]propan-2-ol

https://huagongshe.com/reaction/1455648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantThiazoleHCID 9256—
ReactantTributyltin ChlorideHCID 15096—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-[5-(Tributylstannyl)-1,3-thiazol-2-yl]propan-2-olHCID 46840025—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of thiazole (1.0 eq) in THF (0.2M) at −78° C. was added nBuLi (1.6M, 1.1 eq). After 1 h at −78° C., acetone (1.0 eq) was added and the mixture stirred 30 min at −78° C., 5 min −50° C. then cooled back to −78° C. to add a second equivalent of nBuLi (1.6M, 1.1 eq). After 1.5 h at −78° C., tri-n-butyltin chloride (1.2 eq) was added and the mixture stirred 12 h at −78° C. The reaction mixture was diluted with Et2O and a solution of NH4Cl. The organic extracts were washed with water, brine, dried over MgSO4, filtered and concentrated. Flash chromatography (Hexane:EtOAc, 90:10) afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482456B2
Source datasetuspto-grants-2009_01
ORD IDord-f6ba3af8f1cf4d8f9ace31be503e443d
Source noteuspto-grants-2009_01