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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 744966생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/744966

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물4,4-Dimethyl-2-(4'hydroxymethylbiphenyl-2-yl)oxazolineHCID 11065876—
용매TetrahydrofuranHCID 8028—
생성물4,4-Dimethyl-2-(4'-p-toluenesulfonyloxymethylbiphenyl-2-yl)oxazolineHCID 1538087955%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05559236
출처 데이터셋uspto-grants-1996_09
ORD IDord-355f6135b5d746ebafb58ae165f0d30d
출처 메모uspto-grants-1996_09