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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851220Generated: November 1, 2026

Trimethyl((tributylstannyl)ethynyl)silane → HCID 86630695, compound

https://huagongshe.com/reaction/1851220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl((tributylstannyl)ethynyl)silaneHCID 639663—
ReactantHCID 86630694HCID 86630694—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 86630695HCID 86630695—

Reaction Steps

300 mg 4-(2-bromo-6-phenyl[1,2,4]triazolo[1,5-a]pyrimidin-5-yl)benzaldehyde (prepared as described above), 613 mg trimethyl[(tributylstannyl)ethynyl]silane and 46 mg Pd(PPh3)4 were suspended in 12 mL toluene under a nitrogen atmosphere. The mixture was heated (microwave irradiation) to 120° C. for 1 h. This mixture was worked up by diluting with water and extraction with dichloromethane. The organic layers were dried over Na2SO4 and concentrated to yield the crude product, which was purified by chromatography on silica gel (ethyl acetate/dichloromethane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957064B2
Source datasetuspto-grants-2015_02
ORD IDord-05470eb4bb87437cac1c6566e1e26025
Source noteuspto-grants-2015_02