反应 #4133633
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-524ef965d03848869692dc3f63821206暂无可渲染的结构数据
C1=CC=C(C=C1)CCCC=O产品信息
4-苯丁醛(CAS 18328-11-5)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
可能的应用方向
仅供专业研发与工业用途
数据库编号 29030
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-524ef965d03848869692dc3f63821206反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-058a5dd4273b4228b79c09dfe3452972反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fbc996db9f764fa4914437d4ff8d0b73反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e20e973ebe4d438aaef26063870d8b11反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ced64344e0d146d4ab4561743a1870c9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ba044cb82401488f92a701a1e1d39279反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fcb59c1467bd41e8bf1e2617daabba9f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-09eb79bd4dc24e3d85c74fe9f34a56f4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-phenylbutanol (1 g) in dichloromethane (35 mL) at 0° C. was added PDC (7.5 g). The resulting suspension was stirred for 2 h at room temperature. The reaction solution was then filtered through a pad of silica gel. Concentration of the filtrate and flash chromatography of the residue (20% ethyl acetate/hexanes) provided 4-phenylbutanal (237 mg) as a colorless oil. The reaction solution was then filtered through a pad of silica gel
来源 ID: ord-cb074581c4914473b793136777e8dfa7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a stirred suspension of 4-phenylbutyronitrile (21.7 g, 0.12 mole) in ether (400 ml) at 78° C. is added 85 ml. of 25.3% diisobutylaluminum hydride in toluene over a period of 1 hour. After an additional 1 hour, the dry ice-acetone bath is removed and the reaction mixture is stirred at ambient temperature for 3 hours. The reaction mixture is added slowly to 5% aqueous sulfuric acid and then is extracted with several portions of ether. The ether extracts are combined, washed with water and saturated aqueous sodium chloride solution and dried over magnesium sulfate. After removal of the ether, the residual yellow oil is distilled in vacuo to give an oil. is added 85 ml the dry ice-acetone bath is removed The reaction mixture is added slowly to 5% aqueous sulfuric acid is extracted with several portions of ether washed with water and saturated aqueous sodium chloride solution dried over magnesium sulfate After removal of the ether the residual yellow oil is distilled in vacuo to give an oil
来源 ID: ord-1ecd178d48b140dd8a52050c016d8730反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-524ef965d03848869692dc3f63821206反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-524ef965d03848869692dc3f63821206PubChem References
以下资料来自该化合物的公开数据库参考记录。
相关产品
10 related records
CAS 3318-61-4
CAS 2550-26-7
CAS 121784-15-4
CAS 5406-12-2
CAS 104-53-0
CAS 104175-15-7
CAS 7774-79-0
CAS 5396-91-8
CAS 36884-28-3
CAS 1254940-87-8
