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HRID 1922061作成日:2026年10月27日

Butanal → 2-Ethyl-4-methyl-1,3-oxathiane

https://huagongshe.com/reaction/1922061

反応式

関与物質

役割名称HCID仕込み量
反応物ButanalHCID 261—
反応物p-Toluenesulfonic acidHCID 6101—
反応物3-Sulfanylbutan-1-olHCID 6430893—
溶媒DichloromethaneHCID 6344—
生成物2-Ethyl-4-methyl-1,3-oxathianeHCID 46195361—

反応手順

A solution of 3-mercapto-1-butanol (106 g, 1 mol, synthesized as above) and PTSA (paratoluenesulfonic acid monohydrate, 38 g, 0.2 mol, commercially available from Sigma-Aldrich, Inc.) in 400 mL of CH2Cl2 (dichloromethane) were cooled with an ice bath. Butyraldehyde (106 mL, 1,2 mol, commercially available from Sigma-Aldrich, Inc.) was added drop wise to the solution, and the reaction mixture was stirred with cooling for half an hour and at room temperature for another 1 hour. The reaction mixture was washed twice with saturated sodium bicarbonate solution and once with brine. The organic phase was then dried with anhydrous magnesium sulfate. The solvent was removed with a rotary evaporator and the crude product was distilled under vacuum to provide 2-ethyl-4-methyl-1,3-oxathiane (98 g), which had a boiling point of 80° C. at a pressure of 10.4 mmHg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08173822B2
出典データセットuspto-grants-2012_05
ORD IDord-1b0f5433964b4bfd924d03e1abb8d17d
出典メモuspto-grants-2012_05