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4-Toluenesulfonyl chloride → 1,6-Di-O-(p-toluenesulphonyl)-2,5-anhydro-D-mannitol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| 反応物 | 2,5-anhydro-D-mannitol | HCID 73544 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 1,6-Di-O-(p-toluenesulphonyl)-2,5-anhydro-D-mannitol | HCID 14076916 | — |
反応手順
5.33 g (27.945 mmol) of p-toluenesulphonyl chloride were added at 0° C. to a solution of 2.16 g (13.15 mmol) of 2,5-anhydro-D-mannitol in 88 ml of pyridine. The mixture was heated to room temperature and stirred for a further 24 hours. The reaction was hydrolysed using ice-water and extracted using CH2Cl2, and the combined organic phases were washed with 3N HCl and NaCl. After drying over MgSO4, the solvent was subsequently removed under reduced pressure. The crude product was purified by means of column chromatography (hexane/ethyl acetate 1:2). Yield: 3.00 g (48% of theory).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07193092B2 |
| 出典データセット | uspto-grants-2007_03 |
| ORD ID | ord-0dd59ae4d97a4658b66d6ba2925c3377 |
| 出典メモ | uspto-grants-2007_03 |