反应 #4164102
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-5dd6d24f7c0e43d39512d3ad99d11186暂无可渲染的结构数据
C1COCCN1C(=O)C(C2=CC=CC=C2)N中间体产品
2-amino-1-morpholin-4-yl-2-phenylethanone
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-amino-1-(morpholin-4-yl)-2-phenylethan-1-one |
|---|---|
| English name | 2-amino-1-morpholin-4-yl-2-phenylethanone |
| IUPAC 名称 | — |
| CAS号 | 877125-77-4 |
| 数据库编号 | 24701957 |
| 分子式 | — |
| 分子量 | — |
产品信息
2-amino-1-(morpholin-4-yl)-2-phenylethan-1-one(CAS 877125-77-4)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 24701957
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
8 条反应 · 8 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5dd6d24f7c0e43d39512d3ad99d11186反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-661d9cceb02a4f29a0d6ac7d4ccf3512反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5dd6d24f7c0e43d39512d3ad99d11186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 LAH (6.1 mmol) in THF (25 mL) is added dropwise a solution of 2-amino-1-morpholin-4-yl-2-phenylethanone (670 mmol) in THF (5 mL) at 0° C. The reaction mixture is refluxed for 2 hr, and then the reaction is quenched by the addition of Na2SO4-10H2O at 0° C. After stirring at room temperature for 0.5 h, the resulting mixture is filtered through celite, and the filtrate is concentrated in vacuo to give the title compound, which is directly used for the next reaction without further purification. The reaction mixture is refluxed for 2 hr the reaction is quenched by the addition of Na2SO4-10H2O at 0° C the resulting mixture is filtered through celite the filtrate is concentrated in vacuo
来源 ID: ord-b9c16faaa6f04945b531ba909df66c3b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 LAH (6.1 mmol) in THF (25 mL) is added dropwise a solution of 2-amino-1-morpholin-4-yl-2-phenylethanone (670 mmol) in THF (5 mL) at 0° C. The reaction mixture is refluxed for 2 hr, and then the reaction is quenched by the addition of Na2SO4-10H2O at 0° C. After stirring at room temperature for 0.5 h, the resulting mixture is filtered through celite, and the filtrate is concentrated in vacuo to give the title compound, which is directly used for the next reaction without further purification. The reaction mixture is refluxed for 2 hr the reaction is quenched by the addition of Na2SO4-10H2O at 0° C the resulting mixture is filtered through celite the filtrate is concentrated in vacuo
来源 ID: ord-b9c16faaa6f04945b531ba909df66c3b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of (2-morpholin-4-yl-2-oxo-1-phenylethyl)carbamic acid tert-butyl ester (3.0 mmol) in CH2Cl2 (6.0 mL) is added TFA (2.0 mL) at 0° C. After stirring at room temperature for 24 h, the reaction mixture is basified to pH 8 with sat. aq NaHCO3. The mixture is extracted with CH2Cl2, and then the combined organic extracts are dried over Na2SO4 and concentrated in vacuo to give the title compound; 1H NMR (CDCl3) δ 2.02 (s, 2H), 3.09-3.14 (m, 1H), 3.20-3.25 (m, 1H), 3.34-3.40 (m, 1H), 3.46-3.60 (m, 3H), 3.65-3.71 (m, 1H), 3.74-3.80 (m, 1H), 7.27-7.34 (m, 5H). The mixture is extracted with CH2Cl2 the combined organic extracts are dried over Na2SO4 concentrated in vacuo
来源 ID: ord-4d3c0ccf77004ad2a9b86a0b85094e09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 LAH (6.1 mmol) in THF (25 mL) is added dropwise a solution of 2-amino-1-morpholin-4-yl-2-phenylethanone (670 mmol) in THF (5 mL) at 0° C. The reaction mixture is refluxed for 2 hr, and then the reaction is quenched by the addition of Na2SO4-10H2O at 0° C. After stirring at room temperature for 0.5 h, the resulting mixture is filtered through celite, and the filtrate is concentrated in vacuo to give the title compound, which is directly used for the next reaction without further purification. The reaction mixture is refluxed for 2 hr the reaction is quenched by the addition of Na2SO4-10H2O at 0° C the resulting mixture is filtered through celite the filtrate is concentrated in vacuo
来源 ID: ord-b9c16faaa6f04945b531ba909df66c3b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of (2-morpholin-4-yl-2-oxo-1-phenylethyl)carbamic acid tert-butyl ester (3.0 mmol) in CH2Cl2 (6.0 mL) is added TFA (2.0 mL) at 0° C. After stirring at room temperature for 24 h, the reaction mixture is basified to pH 8 with sat. aq NaHCO3. The mixture is extracted with CH2Cl2, and then the combined organic extracts are dried over Na2SO4 and concentrated in vacuo to give the title compound; 1H NMR (CDCl3) δ 2.02 (s, 2H), 3.09-3.14 (m, 1H), 3.20-3.25 (m, 1H), 3.34-3.40 (m, 1H), 3.46-3.60 (m, 3H), 3.65-3.71 (m, 1H), 3.74-3.80 (m, 1H), 7.27-7.34 (m, 5H). The mixture is extracted with CH2Cl2 the combined organic extracts are dried over Na2SO4 concentrated in vacuo
来源 ID: ord-4d3c0ccf77004ad2a9b86a0b85094e09PubChem References
以下资料来自该化合物的公开数据库参考记录。
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