反应 #4160513
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-ee483b3361bf4aab813ec94ae2d4ab4f暂无可渲染的结构数据
CC(C)(CO)C(C(=O)NC1CCCCC1)O中间体产品
N-cyclohexyl-2,4-dihydroxy-3,3-dimethylbutanamide
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 | N-环己基-2,4-二羟基-3,3-二甲基丁酰胺 |
|---|---|
| English name | N-cyclohexyl-2,4-dihydroxy-3,3-dimethylbutanamide |
| IUPAC 名称 | — |
| CAS号 | 16424-76-3 |
| 数据库编号 | 289865 |
| 分子式 | — |
| 分子量 | — |
产品信息
N-环己基-2,4-二羟基-3,3-二甲基丁酰胺(CAS 16424-76-3)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 289865
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
7 条反应 · 7 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ee483b3361bf4aab813ec94ae2d4ab4f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ee483b3361bf4aab813ec94ae2d4ab4f反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Place N-cyclohexyl-2,4-dihydroxy-3,3-dimethyl-butyramide (2.178 g, 9.51 mmol), triethylamine (2.7 ml, 19.31 mmol) and toluenesulfonyl chloride (3.70 g, 19.21 mmol) in CH2Cl2 (50 mL) at 0° C. Stir for 30 minutes at 0° C. Quench with hexane and warm to room temperature. Filter white precipitate. Strip the solvent and dissolve the residue in 40 ml of dry THF under the nitrogen atmosphere. Add sodium hydride (3.4 g, 85 mmol) and stir at room temperature for 12 hours. Quench the reaction with methanol/water mixture. Extract with ethyl acetate. Wash the extract with brine and dry over magnesium sulfate. Purification by flash chromatography affords 1.25 g (36%) of the title compound: Mass spectrum (apci) m/z=366 (M+H). at 0° C Quench with hexane warm to room temperature Filter white precipitate Strip the solvent and dissolve the residue in 40 ml of dry THF under the nitrogen atmosphere Quench the reaction with methanol/water mixture Extract with ethyl acetate Wash the extract with brine dry over magnesium sulfate Purification by flash chromatography
来源 ID: ord-a2458d88773e4e84a76641c9464a3622反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Place N-cyclohexyl-2,4-dihydroxy-3,3-dimethyl-butyramide (2.178 g, 9.51 mmol), triethylamine (2.7 ml, 19.31 mmol) and toluenesulfonyl chloride (3.70 g, 19.21 mmol) in CH2Cl2 (50 mL) at 0° C. Stir for 30 minutes at 0° C. Quench with hexane and warm to room temperature. Filter white precipitate. Strip the solvent and dissolve the residue in 40 ml of dry THF under the nitrogen atmosphere. Add sodium hydride (3.4 g, 85 mmol) and stir at room temperature for 12 hours. Quench the reaction with methanol/water mixture. Extract with ethyl acetate. Wash the extract with brine and dry over magnesium sulfate. Purification by flash chromatography affords 1.25 g (36%) of the title compound: Mass spectrum (apci) m/z=366 (M+H). at 0° C Quench with hexane warm to room temperature Filter white precipitate Strip the solvent and dissolve the residue in 40 ml of dry THF under the nitrogen atmosphere Quench the reaction with methanol/water mixture Extract with ethyl acetate Wash the extract with brine dry over magnesium sulfate Purification by flash chromatography
来源 ID: ord-a2458d88773e4e84a76641c9464a3622反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Place N-cyclohexyl-2,4-dihydroxy-3,3-dimethyl-butyramide (2.178 g, 9.51 mmol), triethylamine (2.7 ml, 19.31 mmol) and toluenesulfonyl chloride (3.70 g, 19.21 mmol) in CH2Cl2 (50 mL) at 0° C. Stir for 30 minutes at 0° C. Quench with hexane and warm to room temperature. Filter white precipitate. Strip the solvent and dissolve the residue in 40 ml of dry THF under the nitrogen atmosphere. Add sodium hydride (3.4 g, 85 mmol) and stir at room temperature for 12 hours. Quench the reaction with methanol/water mixture. Extract with ethyl acetate. Wash the extract with brine and dry over magnesium sulfate. Purification by flash chromatography affords 1.25 g (36%) of the title compound: Mass spectrum (apci) m/z=366 (M+H). at 0° C Quench with hexane warm to room temperature Filter white precipitate Strip the solvent and dissolve the residue in 40 ml of dry THF under the nitrogen atmosphere Quench the reaction with methanol/water mixture Extract with ethyl acetate Wash the extract with brine dry over magnesium sulfate Purification by flash chromatography
来源 ID: ord-a2458d88773e4e84a76641c9464a3622反应条件: temp:150.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Place 2-hydroxy-3,3-dimethyl-cyclopentanone (1.044 g, 7.86 mmol), cyclohexylamine (1.91 ml, 16.51 mmol) and toluenesulfonic acid monohydrate (0.152 g, 0.1 mmol) in EtOH (4 mL) in a microwave reactor. Stir for 1 hour at 150° C. Quench with 1N HCl and extract with ethyl acetate. Wash the extract with NaHCO3, brine. Dry over magnesium sulfate, filter, and concentrate to afford N-cyclohexyl-2,4-dihydroxy-3,3-dimethyl-butyramide. Quench with 1N HCl extract with ethyl acetate Wash the extract with NaHCO3, brine Dry over magnesium sulfate filter concentrate
来源 ID: ord-97a5dda0d18c43b6a17d06eeefbf8222反应条件: temp:150.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Place 2-hydroxy-3,3-dimethyl-cyclopentanone (1.044 g, 7.86 mmol), cyclohexylamine (1.91 ml, 16.51 mmol) and toluenesulfonic acid monohydrate (0.152 g, 0.1 mmol) in EtOH (4 mL) in a microwave reactor. Stir for 1 hour at 150° C. Quench with 1N HCl and extract with ethyl acetate. Wash the extract with NaHCO3, brine. Dry over magnesium sulfate, filter, and concentrate to afford N-cyclohexyl-2,4-dihydroxy-3,3-dimethyl-butyramide. Quench with 1N HCl extract with ethyl acetate Wash the extract with NaHCO3, brine Dry over magnesium sulfate filter concentrate
来源 ID: ord-97a5dda0d18c43b6a17d06eeefbf8222PubChem References
以下资料来自该化合物的公开数据库参考记录。
