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Pyridine → 1-Vinyl-1-triethylsilanyloxy-cyclopentane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | 1-Ethynyl-1-triethylsiloxycyclopentane | HCID 22639141 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Lindlars catalyst | HCID 131709914 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 1-Vinyl-1-triethylsilanyloxy-cyclopentane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05827883 |
| 出典データセット | uspto-grants-1998_10 |
| ORD ID | ord-6b7f9ff29bc84de2952902d5811c7688 |
| 出典メモ | uspto-grants-1998_10 |