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HRID 40055作成日:2026年10月25日

4-Toluenesulfonyl chloride → Tetrahydrofuran-3-yl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/40055

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3-Furanol, tetrahydro-HCID 9960—
溶媒PyridineHCID 1049—
生成物Tetrahydrofuran-3-yl 4-methylbenzenesulfonateHCID 1383732587.3%

反応手順

To a solution of tetrahydrofuran-3-ol (500 mg, 5.67 mmol) in pyridine (10 ml) at 0° C. was added 4-methylbenzene-1-sulfonyl chloride (1.08 g, 5.67 mmol). The reaction was stirred at room temperature overnight. The reaction was quenched with water, extracted with ethyl acetate. The organic layer was washed with water, brine, dried over Na2SO4 and concentrated in vacuo to yield crude oil (1.2 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524917B2
出典データセットuspto-grants-2013_09
ORD IDord-3cbe48ced7fd4ce0adb13c99eb89e824
出典メモuspto-grants-2013_09