化工社化工社 化学情報印刷レポート · 研究参考用
p-Toluenesulfonic acid → Methyl 3,5-dihydroxy-4-methylbenzoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | 3,5-Dihydroxy-4-methylbenzoic Acid | HCID 2748045 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Methyl 3,5-dihydroxy-4-methylbenzoate | HCID 11458051 | — |
反応手順
3,5-dihydroxy-4-methylbenzoic acid (5.0 g, 29.79 mmol, 1.0 eq) and PTSA (1.13 g, 5.94 mmol, 0.2 eq) were dissolved in 50 ml of methanol, and the mixture was heated to reflux for 6 h. Methanol was evaporated. The resultant solid was washed with 10% sodium bicarbonate solution. The aqueous solution was extracted thrice with ethyl acetate. The combined organic layer was dried over sodium sulphate and evaporated under vacuum. Yield: 5.25 g (96%). 1H NMR (400 MHz, DMSO-d6): δ 1.98 (s, 3H), 3.78 (s, 3H), 6.93 (s, 2H), 9.53 (s, 2H). LCMS: (ES+) m/z=183 (M+H) Method: Column: Phenomenex Luna C18 (4.6×30) mm, 5 micron Mphase A: 10% MeOH-90% H2O-10 mM NH4OAc Mphase B: 90% MeOH-10% H2O-10 mM NH4OAc
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08722688B2 |
| 出典データセット | uspto-grants-2014_05 |
| ORD ID | ord-985194331e0c4f1f94f3e27ce5f13ec6 |
| 出典メモ | uspto-grants-2014_05 |