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HRID 384539作成日:2026年10月24日

Benzaldehyde → 2-Phenyl-1,3-dithiane

https://huagongshe.com/ja/reaction/384539

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物Boron trifluoride etherateHCID 8000—
反応物1,3-PropanedithiolHCID 8013—
溶媒DichloromethaneHCID 6344—
生成物2-Phenyl-1,3-dithianeHCID 2154787%

反応手順

To a solution of benzaldehyde (10.6 g, 100 mmol) and 1,3-propane dithiol in CH2Cl2 (150 mL) at room temperature was dropwise added BF3.Et2O (6.3 mL, 50 mmol) and the resulting mixture was stirred at room temperature for 2 hours. The reaction mixture was then diluted with CH2Cl2, filtered and the filtrate washed with brine, saturated NaHCO3, brine and dried over Na2SO4. The solvent was removed under reduced pressure to afford a white solid, which was recrystallized from a 1:1 mixture of ether and hexane to afford 17.0 g (87%) of the title compound (65) as white crystalline needles. 1H NMR (CDCl3, 400 MHz): δ 1.91 (m, 1H), 2.14 (m, 1H), 2.89 (m, 2H), 3.04 (m, 2H), 5.16 (s, 1H), 7.35-7.28 (m, 3H), 7.46 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367722B2
出典データセットuspto-grants-2013_02
ORD IDord-f472770636b44d42a59342f290c22ba6
出典メモuspto-grants-2013_02