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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746225Generated: November 2, 2026

Tributylphenyltin → HCID 178472765, compound

https://huagongshe.com/reaction/1746225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphenyltinHCID 607632—
ReactantHCID 178472764HCID 178472764—
CatalystHCID 178418903HCID 178418903—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178472765HCID 17847276583.4%

Reaction Steps

[(8-Bromo-6-chloro-4-hydroxy-2-oxo-2H-thiochromene-3-carbonyl)-amino]-acetic acid ethyl ester (22(d)) (500 mg, 1.2 mmol) was dissolved in anhydrous DMF (5 mL). To the solution was added Tributyl-phenyl-stannane (467 uL, 1.43 mmol), bis(triphenylphosphino) palladium(II) dichloride (100 mg, 0.12 mmol) and 4A molecular sieves. The reaction was sealed and the solution was heated to 120 C for 45 minutes. The reaction was cooled, diluted with ethyl acetate (25 mL) and water (25 mL). The organic phase was separated, dried over magnesium sulfate and concentrated residue in vacuo. The residue was filtered through silica to provide the title compound (418 mg) which was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149476B2
Source datasetuspto-grants-2015_10
ORD IDord-d6efe568be14485eb8002efd5dee1ae3
Source noteuspto-grants-2015_10