反应 #4061569
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-131ef1e65cb24f86b71df4172af6304b暂无可渲染的结构数据
CC(C)(C)OC(=O)NC1CCCCC1C(=O)O中间体产品
2-[(2-methylpropan-2-yl)oxycarbonylamino]cyclohexane-1-carboxylic acid
结构、标识符和计算性质已按 CAS 与数据库记录完成匹配。
| 中文名称 | 2-BOC-氨基环己酸 |
|---|---|
| English name | 2-[(2-methylpropan-2-yl)oxycarbonylamino]cyclohexane-1-carboxylic acid |
| IUPAC 名称 | — |
| CAS号 | 220760-49-6 |
| 数据库编号 | 4405994 |
| 分子式 | — |
| 分子量 | — |
产品信息
2-BOC-氨基环己酸(CAS 220760-49-6)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 4405994
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
9 条反应 · 9 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-131ef1e65cb24f86b71df4172af6304b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8d9046d9730e43d386dba19666d70f4a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixed liquid of 2.00 g of (1RS,2SR)-2-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylic acid and 40 ml of dichloromethane were added 1.41 ml of 2-(trimethylsilyl)ethanol, 0.40 g of DMAP, and 2.21 g of WSC in this order, followed by stirring at room temperature for 60 hours. After evaporating the solvent, ethyl acetate was added thereto, followed by washing with water, a 5% aqueous citric acid solution, a saturated aqueous sodium hydrogen carbonate solution, and a saturated aqueous sodium chloride solution in this order. The organic layer was dried over anhydrous magnesium sulfate and the solvent was then evaporated to obtain 2.82 g of 2-(trimethylsilyl)ethyl(1RS,2SR)-2-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylate as a colorless oily substance. After evaporating the solvent, ethyl acetate was added by washing with water The organic layer was dried over anhydrous magnesium sulfate the solvent was then evaporated
来源 ID: ord-e9f87a5d11b045e999928462ac50dab3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixed liquid of 2.00 g of (1RS,2SR)-2-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylic acid and 40 ml of dichloromethane were added 1.41 ml of 2-(trimethylsilyl)ethanol, 0.40 g of DMAP, and 2.21 g of WSC in this order, followed by stirring at room temperature for 60 hours. After evaporating the solvent, ethyl acetate was added thereto, followed by washing with water, a 5% aqueous citric acid solution, a saturated aqueous sodium hydrogen carbonate solution, and a saturated aqueous sodium chloride solution in this order. The organic layer was dried over anhydrous magnesium sulfate and the solvent was then evaporated to obtain 2.82 g of 2-(trimethylsilyl)ethyl(1RS,2SR)-2-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylate as a colorless oily substance. After evaporating the solvent, ethyl acetate was added by washing with water The organic layer was dried over anhydrous magnesium sulfate the solvent was then evaporated
来源 ID: ord-e9f87a5d11b045e999928462ac50dab3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-131ef1e65cb24f86b71df4172af6304b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8d9046d9730e43d386dba19666d70f4a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixed liquid of 2.00 g of (1RS,2SR)-2-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylic acid and 40 ml of dichloromethane were added 1.41 ml of 2-(trimethylsilyl)ethanol, 0.40 g of DMAP, and 2.21 g of WSC in this order, followed by stirring at room temperature for 60 hours. After evaporating the solvent, ethyl acetate was added thereto, followed by washing with water, a 5% aqueous citric acid solution, a saturated aqueous sodium hydrogen carbonate solution, and a saturated aqueous sodium chloride solution in this order. The organic layer was dried over anhydrous magnesium sulfate and the solvent was then evaporated to obtain 2.82 g of 2-(trimethylsilyl)ethyl(1RS,2SR)-2-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylate as a colorless oily substance. After evaporating the solvent, ethyl acetate was added by washing with water The organic layer was dried over anhydrous magnesium sulfate the solvent was then evaporated
来源 ID: ord-50263032e4454b82940c68e135a030f2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixed liquid of 2.00 g of (1RS,2SR)-2-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylic acid and 40 ml of dichloromethane were added 1.41 ml of 2-(trimethylsilyl)ethanol, 0.40 g of DMAP, and 2.21 g of WSC in this order, followed by stirring at room temperature for 60 hours. After evaporating the solvent, ethyl acetate was added thereto, followed by washing with water, a 5% aqueous citric acid solution, a saturated aqueous sodium hydrogen carbonate solution, and a saturated aqueous sodium chloride solution in this order. The organic layer was dried over anhydrous magnesium sulfate and the solvent was then evaporated to obtain 2.82 g of 2-(trimethylsilyl)ethyl(1RS,2SR)-2-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylate as a colorless oily substance. After evaporating the solvent, ethyl acetate was added by washing with water The organic layer was dried over anhydrous magnesium sulfate the solvent was then evaporated
来源 ID: ord-e9f87a5d11b045e999928462ac50dab3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8d9046d9730e43d386dba19666d70f4aPubChem References
以下资料来自该化合物的公开数据库参考记录。
