反应 #4157478
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-999ca06ae76b4c328277a35d526af762暂无可渲染的结构数据
C1=CC=C(C=C1)OS(=O)(=O)N产品信息
苯基 氨基磺酸盐(CAS 19792-91-7)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 11030308
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-999ca06ae76b4c328277a35d526af762反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1fb2d387081446c1bb67e630d1f44bf6反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4f4169ab8aa8463597893ef968dde42b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-be40cdd70aab42809159226d7d363b34反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3b628df2801b4309a5772243fcb183c4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7e90b516863b4fbaa320ab2cf362c174反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 5.9 g (0.05 mole) of (S)-(+)methyl 3-hydroxy-2-methylpropionate, 9.5 g (0.055 mole) of phenyl sulfamate, 25 ml of toluene and 0.5 g of pyridine was heated at reflux for 2 hr. The reaction solution was concentrated under vacuum, and the residue was chromatographed, using silica gel and eluting with 2% methanol in methylene chloride. The desired fractions were concentrated under vacuum to give 3.9 g (40%) of a pale yellow oil. was heated at reflux for 2 hr The reaction solution was concentrated under vacuum the residue was chromatographed eluting with 2% methanol in methylene chloride The desired fractions were concentrated under vacuum
来源 ID: ord-4050e1107da142d9af9b3d58f7c61f7f反应条件: temp:75.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A reaction flask was charged with 43.8 g (0.252 mole) of sulfamic acid, phenyl ester; 12.6 g (0.084 mole) of 4-acetamidophenol, 9 ml of pyridine and 150 ml p-dioxane. The solution was heated at 75° C. for 18 hours. The solution was concentrated to a brown oil. The oil was portioned between 100 ml methylene chloride and 100 ml of 1.0 N sodium bicarbonate. The mixture was refrigerated overnight then filtered to collect 15.8 g of white solid. 1H NMR spectrum indicated pure product but contaminated with sodium bicarbonate. The solid was added to 100 ml H2O and the mixture stirred for one hour. The solid was collected and dried to give 8.4 g of solid, mp 180°-181° C. The solution was concentrated to a brown oil then filtered to collect 15.8 g of white solid The solid was added to 100 ml H2O The solid was collected dried
来源 ID: ord-4d0dcdd11d284f8dbedcbf5f4a12d8e1反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The compound was prepared by procedures of Example 33 from sulfamoyl chloride and phenol in 30% yield as white solid, mp 81°-85° C.
来源 ID: ord-1a499a36f4eb4fc4a3d7681dae892a4d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-999ca06ae76b4c328277a35d526af762反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1fb2d387081446c1bb67e630d1f44bf6反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1fb2d387081446c1bb67e630d1f44bf6PubChem References
以下资料来自该化合物的公开数据库参考记录。
