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HRID 477332作成日:2026年10月24日

Ethanol → Ethyl (4-methylbenzylthio)acetate

https://huagongshe.com/ja/reaction/477332

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物p-Xylyl bromideHCID 7721—
反応物Ethyl ThioglycolateHCID 12185—
反応物Sodium ethoxideHCID 2723922—
溶媒DichloromethaneHCID 6344—
生成物Ethyl (4-methylbenzylthio)acetateHCID 4107274—

反応手順

Ethyl 2-mercaptoacetate (8.5 cc) is added in the course of 15 minutes at a temperature in the region of 20° C. to a stirred solution, through which a stream of nitrogen is passed, of a 2M ethanolic solution of sodium ethylate (37.5 cc) and ethanol (50 cc). The mixture is left with stirring for 15 minutes at the same temperature, and α-bromo-p-xylene (13.9 g) is then added in the course of 20 minutes at a temperature in the region of 20° C. Stirring is maintained for 60 minutes at this temperature, and the reaction mixture is then evaporated to dryness at 50° C. under reduced pressure (20 mm Hg; 2.7 kPa). The residue obtained is dissolved in dichloromethane (100 cc), and the organic phase is dried over anhydrous magnesium sulphate, filtered and concentrated to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa). Ethyl (4-methylbenzylthio)acetate (15.6 g) is thereby obtained, and is used in the crude state in the subsequent syntheses.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04886835
出典データセットuspto-grants-1989_12
ORD IDord-5f945fb988944ca2b579be667497689b
出典メモuspto-grants-1989_12