関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methane | HCID 297 | — |
| 反応物 | 3-[4-[(6-Bromohexyl)oxy]but-1-ynyl}benzenesulfonamide | HCID 21895558 | — |
| 生成物 | Benzenesulfonamide, 3-[4-[(6-bromohexyl)oxy]butyl]- | HCID 21895438 | 78.8% |
反応手順
3-{4-[(6-Bromohexyl)oxy]but-1-ynyl}benzenesulfonamide (627 g) in IMS (1900 ml) was stirred with activated charcoal (314 g) at room temperature for 2 h and then filtered through a short pad of Celite. The filter pad was washed with IMS (4300 ml) and the filtrate transferred to a hydrogenation vessel. 5% Platinum on Charcoal (520.1 g, ˜50% water) was added and the reaction mixture was then stirred under an atmosphere of hydrogen (0.2 bar) at 20° C. for 6 h. The mixture was then filtered through a short pad of Celite and concentrated under reduced pressure to give the title compound (499 g) as a solid, LC RT=5.66 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07402598B2 |
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| 出典データセット | uspto-grants-2008_07 |
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| ORD ID | ord-26fdd124fc37462598b2657b088290bc |
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| 出典メモ | uspto-grants-2008_07 |
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