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HRID 344983作成日:2026年10月26日

1-Eth-1-ynyl-4-(pentyloxy)benzene → 4-(2-(4-Pentoxyphenyl)-ethynyl)-phenyl-sulfur pentafluoride

https://huagongshe.com/reaction/344983

反応式

関与物質

役割名称HCID仕込み量
反応物1-Eth-1-ynyl-4-(pentyloxy)benzeneHCID 2775119—
反応物1-Bromo-4-(pentafluoro-lambda6-sulfanyl)benzeneHCID 2779194—
触媒Copper iodideHCID 83717—
触媒Triphenylphosphine palladium dichlorideHCID 13169693—
溶媒PiperidineHCID 8082—
生成物4-(2-(4-Pentoxyphenyl)-ethynyl)-phenyl-sulfur pentafluorideHCID 86745128—

反応手順

8.5 g of p-bromophenyl-sulfur pentafluoride and 20 ml of piperidine are added to a mixture of 8.5 g of 4-pentoxyphenylacetylene, 20 ml of piperidine, 420 mg of triphenylphosphine-palladium(II) chloride and 30 mg of copper iodide, and the combined mixture is heated for 20 hours. Concentration and working up in the customary manner gives 4-(2-(4-pentoxyphenyl)-ethynyl)-phenyl-sulfur pentafluoride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05055223
出典データセットuspto-grants-1991_10
ORD IDord-d9b160dc297649a4900136f57f6e4fed
出典メモuspto-grants-1991_10