化工社化工社 化学情報印刷レポート · 研究参考用
Tetrahydrofuran → 4-(Methanesulfinyl)-4-(methylsulfanyl)cyclopent-1-ene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Methyl (methylsulfinyl)methyl sulfide | HCID 99129 | — |
| 反応物 | 1,4-Dichloro-cis-2-butene | HCID 6432115 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-(Methanesulfinyl)-4-(methylsulfanyl)cyclopent-1-ene | HCID 13298796 | 61% |
反応手順
Formaldehyde dimethyl mercaptal S-oxide (1.27g) was dissolved in 15 ml. of tetrahydrofuran, and 246 mg of sodium hydride was added. The mixture was stirred for 30 minutes at room temperature, and then for 2 hours at 50° C. With ice cooling, 442 mg of cis-1,4-dichloro-2-butene was added. The mixture was stirred for 1 hour with ice cooling, and then for 6.5 hours at room temperature. Methylene chloride (100 ml) was added, and the insoluble matter was separated by filtration. The filtrate was concentrated at reduced pressure, and the residue was separated by column chromatography (Florisil, eluted with methylene chloride) to afford 382 mg of 3-cyclopentenone dimethyl mercaptal S-oxide in a yield of 61%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04020171 |
| 出典データセット | uspto-grants-1977_04 |
| ORD ID | ord-fb244c2e5890411c8b3edde641ffeb48 |
| 出典メモ | uspto-grants-1977_04 |