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HRID 550328作成日:2026年10月26日

Methane → 1,1,1-Trifluoro-2-trifluoromethyl-5-vinyloxy-pentan-2-ol

https://huagongshe.com/reaction/550328

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物Vinyl AcetateHCID 7904—
反応物Sodium CarbonateHCID 10340—
反応物5,5,5-Trifluoro-4-(trifluoromethyl)pentane-1,4-diolHCID 21895362—
触媒HCID 178478077HCID 178478077—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
生成物1,1,1-Trifluoro-2-trifluoromethyl-5-vinyloxy-pentan-2-olHCID 5876380225%

反応条件

温度100 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947425B2
出典データセットuspto-grants-2011_05
ORD IDord-916deb0365bf4401a69e629fbff88db9
出典メモuspto-grants-2011_05