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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129418Generated: November 2, 2026

Trimethyl((tributylstannyl)ethynyl)silane → HCID 19371473, compound

https://huagongshe.com/reaction/129418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl((tributylstannyl)ethynyl)silaneHCID 639663—
ReactantHCID 19371446HCID 19371446—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 19371473HCID 1937147380%

Reaction Steps

5.4 g of ethyl 8-bromo-1-ethyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate (Example Z22), 10.8 g of tributylstannyl-trimethylsilyl-acetylene and 0.87 g of tetrakis(triphenylphosphine)palladium(0) are refluxed for 24 hours in 50 ml of absolute toluene under a nitrogen atmosphere. The reaction mixture is concentrated, the residue is stirred with 100 ml of hexane, and the resulting solid is filtered off with suction and dried. 4.53 g of ethyl 1-ethyl-6,7-difluoro-1,4-dihydro-8-(trimethylsilylethinyl)-4-oxo-3-quinolinecarboxylate are obtained (80% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468742
Source datasetuspto-grants-1995_11
ORD IDord-c5e79359b82f4dff8661b0aff3a00c6a
Source noteuspto-grants-1995_11