Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915601Generated: October 31, 2026

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

https://huagongshe.com/reaction/1915601

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 under example 53), 613 mg trimethyl[(tributylstannyl)ethynyl]silane and 46 mg Pd(PPh3)4 are suspended in 12 ml toluene under a nitrogen atmosphere. The mixture is heated (microwave irradiation) to 120° C. for 1 h. This mixture is worked up by diluting with water and extraction with dichloromethane. The organic layers are dried over Na2SO4 and concentrated to yield the crude product, which is purified by chromatography on silica gel (ethyl acetate/dichloromethane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614218B2
Source datasetuspto-grants-2013_12
ORD IDord-4fc0b088e6c34804a588c019945ec985
Source noteuspto-grants-2013_12