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HRID 53431作成日:2026年10月26日

4-Toluenesulfonyl chloride → 4,4-Dimethyl-2-(4'-p-toluenesulfonyloxymethylbiphenyl-2-yl)oxazoline

https://huagongshe.com/reaction/53431

反応式

関与物質

役割名称HCID仕込み量
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物Sodium hydrideHCID 24758—
反応物Ammonium ChlorideHCID 25517—
反応物4,4-Dimethyl-2-(4'hydroxymethylbiphenyl-2-yl)oxazolineHCID 11065876—
溶媒TetrahydrofuranHCID 8028—
生成物4,4-Dimethyl-2-(4'-p-toluenesulfonyloxymethylbiphenyl-2-yl)oxazolineHCID 1538087955%

反応手順

0.34 g (8.5 mmol) of a 60% oily sodium hydride was suspended in tetrahydrofuran (20 ml). A solution of 2.0 g (7.1 mmol) of 4,4-dimethyl-2-(4'-hydroxymethylbiphenyl-2-yl)oxazoline in tetrahydrofuran (30 ml) was dropwise added thereto at room temperature, followed by further stirring at room temperature for one hour. After the reaction liquid was cooled with ice, a solution of 1.6 g (8.4 mmol) of p-toluenesulfonyl chloride in tetrahydrofuran (20 ml) was dropwise added thereto. After stirring for 3 hours as such, the reaction liquid was poured into a saturated aqueous solution of ammonium chloride, followed by the extraction with chloroform. After washing with water and drying, vacuum concentration was conducted. The residue was purified by silica gel column chromatography (a n-hexane/ethyl acetate system) to give 1.7 g of the title compound as an oil (yield 55%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05618969
出典データセットuspto-grants-1997_04
ORD IDord-5c35ca7d30c946a69c9c95931527d5b9
出典メモuspto-grants-1997_04