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HRID 861836作成日:2026年10月26日

Triethylamine → 2-Methanesulfonyloxy-2-p-tolyl-1,1,1,3,3,3-hexafluoropropane

https://huagongshe.com/reaction/861836

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物2-(p-Tolyl)hexafluoroisopropanolHCID 74829—
溶媒DichloromethaneHCID 6344—
生成物2-Methanesulfonyloxy-2-p-tolyl-1,1,1,3,3,3-hexafluoropropaneHCID 1970027371.4%

反応条件

温度5 °C

反応手順

5.16 g (20 mmol) of 1,1,1,3,3,3-hexafluoro-2-p-tolylpropan-2-ol were dissolved in 50 ml of methylene chloride, and 2.8 g (28 mmol) of triethylamine were added. 3.2 g (22 mmol) of methanesulfonyl chloride were added dropwise, while stirring, to the solution cooled to 5° C. After warming up to room temperature, the mixture was allowed to stand overnight. The precipitated salt was filtered off and the organic solution was evaporated down. The subsequent chromatography (silica gel/methylene chloride) gave 4.8 g of 2-methanesulfonyloxy-2-p-tolyl-1,1,1,3,3,3-hexafluoropropane (pale yellow oil).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05716756
出典データセットuspto-grants-1998_02
ORD IDord-bfa83e74d423487693db90f92360767b
出典メモuspto-grants-1998_02