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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362371Generated: October 30, 2026

Tributyltin Chloride → HCID 15288193, compound

https://huagongshe.com/reaction/362371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactantalpha-Bromo-2-nitrotolueneHCID 77569—
Reactant4,5-dihydro-4,4-dimethyl-2-(2-thienyl)-oxazoleHCID 5008282—
ReactantHCID 15288192HCID 15288192—
ReactantButyllithiumHCID 178418339—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 15288193HCID 15288193—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4,5-dihydro-4,4-dimethyl-2-(2-thienyl)-oxazole (4.5 gms 25 mmol) in anhydrous ether at -70° C., n-butyl-lithium (2.5 molar solution in hexane, 11 ml) is added drop by drop under N2 atmosphere. The reaction mixture is stirred at -78° C. for 45 minutes and tri-n-butyltin chloride (8.3 gms 25 mmol) in dry ether is added drop by drop. The reaction mixture is stirred at room temperature for 1 hour and quenched with water. The reaction mixture is extracted with ether, washed well with water, dried and concentrated. The product obtain is pure enough for further transformation. The oil product, 4,5-dihydro-4,4-dimethyl-2-[3-(tributylstannyl)-2-thienyl]-oxazole is mixed with 2-nitrobenzyl bromide (5.5 g 25 mmol) in toluene and refluxed in the presence of tetrakis (triphenylphosphine)-palladium (0) (200 mg) for 16 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869483
Source datasetuspto-grants-1999_02
ORD IDord-dd239aaa3f594480b247f768f22cde37
Source noteuspto-grants-1999_02