関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methane | HCID 297 | — |
| 反応物 | Vinyl Acetate | HCID 7904 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 5,5,5-Trifluoro-4-(trifluoromethyl)pentane-1,4-diol | HCID 21895362 | — |
| 触媒 | HCID 178478077 | HCID 178478077 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 1,1,1-Trifluoro-2-trifluoromethyl-5-vinyloxy-pentan-2-ol | HCID 58763802 | 25% |
反応手順
1,1,1-Trifluoro-2-trifluoromethyl-2,5-pentanediol (11.3 g, 50 mmol), toluene (50 mL), sodium carbonate (10.6 g,100 mmol), chloro-1,5-cyclooctadiene iridium(I) dimer (0.34 g, 0.5 mmol), vinyl acetate(14 mL, 150 mmol) were placed in a dry 250 mL round-bottom flask equipped with a stir bar, condenser, and nitrogen inlet. The reaction mixture was heated to 100° C. and stirred for 3 hours, after which time it was cooled to room temperature. Diethyl ether (50 mL) was added to quench the reaction. After adding charcoal, the mixture was stirred for 1 hr and filtered with Celite 521. Diethyl ether, excess vinyl acetate, and solvent were distilled off under reduced pressure. The degree of the transetherification of the primary diol was found to be 52% by GC. Vacuum distillation (68-70° C., 15 mm Hg) afforded 3.13 g (25%) of colorless liquid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07947425B2 |
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| 出典データセット | uspto-grants-2011_05 |
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| ORD ID | ord-916deb0365bf4401a69e629fbff88db9 |
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| 出典メモ | uspto-grants-2011_05 |
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