戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1530796作成日:2026年10月27日

Vinylidene fluoride → 8-(2,2,2-Trifluoroethylidene)-1,4-dioxaspiro[4.5]decane

https://huagongshe.com/reaction/1530796

反応式

関与物質

役割名称HCID仕込み量
反応物Vinylidene fluorideHCID 6369—
反応物1,4-Dioxaspiro(4.5)decaneHCID 9093—
反応物Ammonium ChlorideHCID 25517—
反応物(Diethylamino)sulfur trifluorideHCID 123472—
反応物CID 53628100HCID 178418400—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物8-(2,2,2-Trifluoroethylidene)-1,4-dioxaspiro[4.5]decaneHCID 21252678—

反応条件

温度-100 °C

反応手順

At −100° C., 22 g of 1,1-difluoroethylene were condensed into a solvent mixture of 400 ml of tetrahydrofuran and 100 ml of diethyl ether. Subsequently, 153 ml of a 1.3 molar solution of sec-BuLi were added dropwise to the reaction solution at a temperature between −90° C. and −100° C. Finally, 31.2 g of 1,4-dioxaspiro[4.5]decane were added, the solution was stirred at −100° C. for another 20 minutes and subsequently warmed to 0° C. with stirring. The reaction solution was poured into an aqueous ammonium chloride and extracted with methylene chloride and the combined organic phases were dried over magnesium sulfate and concentrated. The residue was taken up in 400 ml of methylene chloride and, at −70° C., reacted with 32 g (0.2 mol) of DAST, dissolved in 100 ml of methylene chloride. The mixture was then slowly warmed to 0° C. with stirring, and the reaction solution was subsequently poured into an aqueous ammonium chloride. The product was extracted with diethyl ether and the combined organic phases were dried over MgSO4 and concentrated. The residue was chromatographed over silica gel (petroleum ether/ethyl acetate 4:1), to give the title product as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06197729B1
出典データセットuspto-grants-2001_03
ORD IDord-06c96a7b378a45e7b9a3621bb1afbcb6
出典メモuspto-grants-2001_03