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HRID 1703作成日:2026年10月23日

Carbon Dioxide → 2,2,2-Trifluoroethyl trifluoromethanesulfonate

https://huagongshe.com/ja/reaction/1703

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物2,2,2-TrifluoroethanolHCID 6409—
反応物TriethylamineHCID 8471—
反応物Trifluoromethanesulfonyl chlorideHCID 79000—
溶媒Diethyl EtherHCID 3283—
溶媒IsopropanolHCID 3776—
溶媒DichloromethaneHCID 6344—
生成物2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—

反応条件

温度0 °C

反応手順

A solution of trifluoromethanesulfonyl chloride (800 uL, 7.5 mmole) in CH2Cl2 (6 mL) was cooled under argon to -60° C. (IPA:dry ice bath). 2,2,2-Trifluoroethanol was added (456 uL, 6 mmol) and triethylamine (1.04 uL, 7.5 mmol) was added dropwise. The reaction was stirred for 1.5 hours then warmed to 0° C. for 1 hour. Anhydrous ether (20 mL) was added and the mixture was stirred at 0° C. for 30 minutes. The solids were filtered off and the solvent was removed under reduced pressure with the flask maintained at 0° C. This afforded the 2,2,2-trifluoroethyltriflate as a yellow oil which was used immediately.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726172
出典データセットuspto-grants-1998_03
ORD IDord-c1eb50330c204669ac80b93517bb8dec
出典メモuspto-grants-1998_03