関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Phenylacetaldehyde | HCID 998 | — |
| 反応物 | Boron trifluoride etherate | HCID 8000 | — |
| 反応物 | 1,3-Propanedithiol | HCID 8013 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Benzyl-1,3-dithiane | HCID 300291 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05180733 |
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| 出典データセット | uspto-grants-1993_01 |
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| ORD ID | ord-2b9fd1d276aa4a9cbdfac5a9fefc4f71 |
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| 出典メモ | uspto-grants-1993_01 |
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