参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | ubiquitin cross-reactive protein | HCID 311 | — |
| 反应物 | 5-氰基-2-糠醛 | HCID 642139 | — |
| 反应物 | 硼氢化钠 | HCID 4311764 | — |
| 溶剂 | 乙醇 | HCID 702 | — |
| 溶剂 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 产物 | 5-(羟甲基)呋喃-2-甲腈 | HCID 3021406 | 8,800% |
反应步骤
2.34 g (62 mmol) of sodium borohydride were added in portions to a solution of 30 g (0.25 mol) of 5-cyanofuran-2-carbaldehyde in 500 ml of absolute ethanol at -30° C. The solution was stirred at -30° C. for 2 hours and, while cooling, was adjusted to pH 7 with a 5% strength citric acid solution in water. The reaction mixture was concentrated under water pump vacuum, saturated sodium chloride solution was added to the residue, the mixture was extracted several times with 150 ml of diethyl ether each time, the combined organic phases were dried over magnesium sulfate, the desiccant was filtered off, and the solvent was distilled off under water pump vacuum at room temperature. This resulted in 27 g (22 mol, 88%) of the title compound as a dark red oil, which was employed without further purification in the following reactions. 1H-NMR (250 MHz, d6 -DMSO): δ=4.4 (m, 2H), 5.6 (bs, 1H), 6.6 (d, 1H), 7.5 (d, 1H).
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 专利号 | US06114358 |
|---|
| 来源数据集 | uspto-grants-2000_09 |
|---|
| ORD ID | ord-595a70d2fddd4cb0852a24aab3c4685d |
|---|
| 来源说明 | uspto-grants-2000_09 |
|---|