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p-Toluenesulfonic acid → 3-[1,3]Dioxan-2-yl-2'-methyl-biphenyl-4-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | 1,3-Propanediol | HCID 10442 | — |
| 反応物 | 4-Hydroxy-2'-methyl[1,1'-biphenyl]-3-carbaldehyde | HCID 20099867 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 3-[1,3]Dioxan-2-yl-2'-methyl-biphenyl-4-ol | HCID 69217629 | 89% |
反応手順
A solution of 4-hydroxy-2′-methyl-biphenyl-3-carbaldehyde (18.8 mmol) in toluene (100 mL) was added 1,3-dihydroxypropane (65.7 mmol) and p-toluenesulfonic acid (cat) and heated at reflux overnight in a Dean-Stark set-up. The reaction was cooled and washed with a solution of Na2CO3 (aq, 1 M). Evaporation in vacuo gave the title product as brown oil in 89% yield. 1H-NMR (CDCl3) δ 9.61 (bs, 1H), 7.34-7.10 (m, 6H), 6.87 (d, 1H), 5.77 (s,1H), 4.13-4.07 (m, 2H), 3.95-3.86 (m, 2H), 2.20 (s, 3H), 2.18-1.96 (m, 1H), 1.40 (d, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07423181B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-12868647474649d7a47cf0fd64862070 |
| 出典メモ | uspto-grants-2008_09 |