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HRID 358430作成日:2026年10月26日

4-Toluenesulfonyl chloride → HCID 178427745、化合物

https://huagongshe.com/reaction/358430

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(4-Phenylcyclohexyl)methanolHCID 3100608—
溶媒PyridineHCID 1049—
溶媒TolueneHCID 1140—
生成物HCID 178427745HCID 17842774585%

反応条件

温度5 °C

反応手順

The compound (III) (50 g, 0.268 mol) obtained in the first step was dissolved in dry pyridine (110 ml) and the solution was cooled to 5° C. or lower. To this solution was dropwise added a solution of p-toluenesulfonic acid chloride (50.1 g, 0.263 mol) dissolved in dry toluene (70 ml), in small portions through a dropping funnel so that the reaction temperature did not exceed 10° C. After completion of the dropwise addition, the cooling bath was removed and the reaction mixture was agitated at room temperature for 4 hours, followed by adding water (100 ml) and toluene (300 ml) and stirring. The mixture was transferred into a separating funnel and the toluene layer was washed twice with 6N-HCl aqueous solution (100 ml), then once with water (200 ml), further twice with 2N-NaOH aqueous solution (100 ml) and then four times with water (200 ml). Toluene was distilled off under reduced pressure and the resulting crystals were recrystallized from toluene (90 ml), followed by separating the crystals by filtration to obtain p-toluenesulfonic acid (trans-4-phenylcyclohexylmethyl) ester (IV) (77 g) having a melting point of 108.0°~108.7° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04468340
出典データセットuspto-grants-1984_08
ORD IDord-f4a6729955f3448988f1c020e080f99c
出典メモuspto-grants-1984_08