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HRID 2186372作成日:2026年10月25日

Water → 2-Hydroxyethyl cycloheptyl sulfide

https://huagongshe.com/reaction/2186372

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-MercaptoethanolHCID 1567—
反応物BromocycloheptaneHCID 16992—
反応物Sodium hydrideHCID 24758—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物2-Hydroxyethyl cycloheptyl sulfideHCID 2245407392.9%

反応手順

2.32 g of 2-mercaptoethanol, dissolved beforehand in 10 cm3 of dimethylformamide, were slowly added, under an inert atmosphere and at a temperature in the region of 20° C., to a stirred suspension of 0.91 g of 60% sodium hydride in 10 cm3 of anhydrous dimethylformamide. After stirring for 20 minutes, 3.5 g of bromocycloheptane, dissolved in 10 cm3 of dimethylformamide, were added. The reaction was brought to completion by stirring at a temperature in the region of 20° C. for 1 hour 30 minutes. The reaction mixture was poured onto 150 cm3 of water to which have been added 100 cm3 of diethyl ether. The ethereal phase was separated by settling and the aqueous phase was extracted once with 50 cm3 of diethyl ether. The organic phases were combined and then washed with 2 times 100 cm3 of water, dried over magnesium sulfate, filtered, and concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C. 3.2 g of 2-hydroxyethyl cycloheptyl sulfide were obtained in the form of an oil with a yellow color.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06403610B1
出典データセットuspto-grants-2002_06
ORD IDord-c15893eda1a044219750fd1658c36fda
出典メモuspto-grants-2002_06