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HRID 78487作成日:2026年10月25日

4-Toluenesulfonyl chloride → (Oxan-3-yl)methyl 4-methylbenzene-1-sulfonate

https://huagongshe.com/reaction/78487

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Tetrahydro-2H-pyran-3-methanolHCID 85769—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物(Oxan-3-yl)methyl 4-methylbenzene-1-sulfonateHCID 86618913—

反応手順

To a solution of (tetrahydropyran-3-yl)-methanol (Matrix, 1.67 g, 14.4 mmol) in 15 mL of CH2Cl2 and 15 mL of pyridine was added p-toluenesulfonyl chloride (2.9 g, 15.1 mmol) in portions over 10 minutes. The mixture stirred at ambient temperature for 18 hours and was quenched with 10 mL of saturated, aqueous NaHCO3. The layers were separated and the aqueous phase was extracted three 5 mL of portions of CH2Cl2. The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Purification via column chromatography (SiO2, 70% hexanes in ethyl acetate) afforded the title compound. MS (DCI/NH3) m/z 288 (M+NH4)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841334B2
出典データセットuspto-grants-2014_09
ORD IDord-25715a1446204b478a238d2771de1968
出典メモuspto-grants-2014_09