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HRID 1646580作成日:2026年10月26日

Phenylacetaldehyde → 2-Benzyl-1,3-dithiane

https://huagongshe.com/reaction/1646580

反応式

関与物質

役割名称HCID仕込み量
反応物PhenylacetaldehydeHCID 998—
反応物Boron trifluoride etherateHCID 8000—
反応物1,3-PropanedithiolHCID 8013—
反応物Potassium HydroxideHCID 14797—
溶媒DichloromethaneHCID 6344—
生成物2-Benzyl-1,3-dithianeHCID 30029191%

反応手順

To a solution of 33.9 g (280 mmol) of phenylacetaldehyde and 35.6 g (330 mmol) of 1,3-propanedithiol in 300 mL of methylene chloride at 0° C., was added, dropwise over a period of 30 minutes, 10 mL of boron trifluoride etherate. The reaction mixture was allowed to warm to ambient temperature and stirred for 3 h at ambient temperature. The reaction mixture was made basic by the addition of 180 mL of 5% aqueous potassium hydroxide solution and the resultant mixture was stirred for 0.5 h. The layers were separated and the aqueous layer was extracted with methylene chloride. The combined organic extract was washed with 1N aqueous sodium hydroxide solution and brine, dried over anhydrous magnesium sulfate, filtered and the filtrate was distilled to afford 53.62 g (91% yield) of the title compound, b.p. 150° C. (2 mm Hg); 1H NMR (CDCl3) δ1.75-1.95 (1H, m), 2.05-2.17 (1H, m), 2.75-2.91 (4H, m), 3.03 (2H, d, J=9 Hz), 4.25 (1H, t, J=9 Hz), 7.17-7.38 (5H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05180733
出典データセットuspto-grants-1993_01
ORD IDord-2b9fd1d276aa4a9cbdfac5a9fefc4f71
出典メモuspto-grants-1993_01