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p-Toluenesulfonic acid → 4-(2,3-Dihydrothieno[3,4-b][1,4]dioxin-2-yl)-1-butanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | 1,2,6-Hexanetriol | HCID 7823 | — |
| 反応物 | 3,4-Di-n-propoxythiophene | HCID 11401397 | — |
| 生成物 | 4-(2,3-Dihydrothieno[3,4-b][1,4]dioxin-2-yl)-1-butanol | HCID 22590342 | — |
反応手順
9.06 g (45.2 mmol) of 3,4-di-n-propoxythiophene, 30.3 g (226 mmol) of 1,2,6-hexanetriol and 0.09 g (0.5 mmol) of p-toluenesulphonic acid are heated to 150 to 165° C. (bath temperature) under N2 for 3 h. During this time, 5.8 g of distillate (substantially n-propanol) were collected. The cooled liquid was diluted with 50 ml of methylene chloride, washed to neutrality and to free it of hexanetriol with water and the organic phase was dried over Na2SO4. After filtering and evaporating the methylene chloride, the residue (6.73 g=74.8% of theory) was identified by 1H NMR spectroscopy (in CDCl3 against TMS) using δ=6.30 ppm (2H, thiophene H) and 2.85 ppm (1H, OH) as being substantially 4-(2,3-dihydrothieno[3,4-b][1,4]dioxin-2-yl)-1-butanol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06852831B2 |
| 出典データセット | uspto-grants-2005_02 |
| ORD ID | ord-d92287d6b2ae41aa84fbe9104e260357 |
| 出典メモ | uspto-grants-2005_02 |