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1,3-Cyclohexadiene → 5,6-Di(benzenesulfonyl)bicyclo[2.2.2]oct-2-ene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,3-Cyclohexadiene | HCID 11605 | — |
| 反応物 | trans-1,2-Bis(phenylsulfonyl)ethylene | HCID 5367099 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 5,6-Di(benzenesulfonyl)bicyclo[2.2.2]oct-2-ene | HCID 12778411 | 104.6% |
反応手順
A mixed solution of 3.16 g (39.5 mmol) of 1,3-cyclohexadiene, 10.5 g (34.05 mmol) of trans-1,2-bis(phenylsulfonyl)ethylene, and 200 ml of toluene was refluxed for 7 hours. Then, the mixed solution was cooled and concentrated under reduced pressure to yield a reaction mixture. The reaction crude product was recrystallized (chloroform/hexane) to yield 5,6-bis(phenylsulfonyl)-bicyclo[2,2,2]octa-2-ene (13.8 g, 35.6 mmol, 90% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07863081B2 |
| 出典データセット | uspto-grants-2011_01 |
| ORD ID | ord-f835a53e818f45ccbbdb0154d064146b |
| 出典メモ | uspto-grants-2011_01 |