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HRID 400219作成日:2026年10月26日

Pyridine → 1-Vinyl-1-triethylsilanyloxy-cyclopentane

https://huagongshe.com/reaction/400219

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物1-Ethynyl-1-triethylsiloxycyclopentaneHCID 22639141—
反応物HCID 178418361HCID 178418361—
触媒Lindlars catalystHCID 131709914—
溶媒HexaneHCID 8058—
生成物1-Vinyl-1-triethylsilanyloxy-cyclopentaneHCID 18944493—

反応手順

Lindlar catalyst (250 mg) was prehydrogenated in hexane (40 ml) and pyridine (0.25 ml) for 30 min.; after addition of 1-Ethinyl-1-triethylsilanyloxy-cyclopentane (11.22 g; 50.0 mmole) dissolved in hexane (80 ml) hydrogenation was continued at ambient temperature and normal pressure until the uptake of hydrogen ceased; the catalyst was removed by filtration through a plug of neutral alumina (act. 3); after removal of the solvent under reduced pressure the crude product was purified by distillation. 1-Vinyl-1-triethylsilanyloxy-cyclopentane (B1) was obtained as a colourless oil; bp.: 100° C. (0.2 mbar), Kugelrohr.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05827883
出典データセットuspto-grants-1998_10
ORD IDord-6b7f9ff29bc84de2952902d5811c7688
出典メモuspto-grants-1998_10