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HRID 257848作成日:2026年10月27日

Water → 4-(Ethylthio)benzyl alcohol

https://huagongshe.com/reaction/257848

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium HydroxideHCID 14798—
反応物4-(Ethylthio)benzoic acidHCID 83231—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒TetrahydrofuranHCID 8028—
生成物4-(Ethylthio)benzyl alcoholHCID 53363886.6%

反応条件

温度0 °C

反応手順

The starting 4-(ethylthio)benzyl alcohol was prepared as follows. A mixture of lithium aluminum hydride (5.2 g) and tetrahydrofuran (250 mL) was cooled to 0° C. with stirring under N2 atmosphere. A solution of 4-(ethylthio)benzoic acid (25 g) in tetrahydrofuran (300 mL) was added at a rate so as to control H2 evolution. The reaction mixture was then allowed to warm to room temperature and stirred 15 hours. The mixture was cooled in ice and a solution of 15% aqueous sodium hydroxide solution was added, (6 mL) followed by water (21 mL). The mixture was stirred at ice temperature for 1 hour and for 2 hours at ambient temperature. The solution was decanted, diluted with diethyl ether and washed with saturated aqueous NaCl solution. The organic phase was dried over MgSO4, filtered through a celite pad and concentrated to give 4-(ethylthio)benzyl alcohol (20 g). This material was converted to the corresponding bromide as in Example 1 except that diethyl ether and hexane were used for the triturations rather than heptane and petroleum ether, respectively.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05264451
出典データセットuspto-grants-1993_11
ORD IDord-04f09ebae8b4406697d7343bab8bb06c
出典メモuspto-grants-1993_11