反应 #3882720
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-032fe7ec07a0430291eac5ac4dd7cc78暂无可渲染的结构数据
C1=CC=C(C(=C1)CC(C(=O)N)N)F产品信息
2-氨基-3-(2-氟苯基)丙酰胺(CAS 208655-11-2)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。
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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-032fe7ec07a0430291eac5ac4dd7cc78反应条件: temp:5.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-Amino-3-(2-fluorophenyl)propionamide was added carefully to a chilled (5°) mixture of LAH (1.0 g, 26.3 mmol) and 20 ml THF under argon. The reaction was then heated at reflux for 10 hrs. The reaction was cooled to 5° C. and carefully treated with Na2SO4.10 H2O. The resulting mixture was stirred for 18 hrs, then filtered to remove the solids. The filtrate was concentrated in vacuo to give an amber oil. MS (m/z): 169 (M+H)+; C9H13FN2 requir. 168.19 a chilled The reaction was then heated at reflux for 10 hrs filtered to remove the solids The filtrate was concentrated in vacuo to give an amber oil
来源 ID: ord-29fe5172f9d94884869e0ed43b282c11反应条件: temp:5.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-Amino-3-(2-fluorophenyl)propionamide was added carefully to a chilled (5°) mixture of LAH (1.0 g, 26.3 mmol) and 20 ml THF under argon. The reaction was then heated at reflux for 10 hrs. The reaction was cooled to 5° C. and carefully treated with Na2SO4.10 H2O. The resulting mixture was stirred for 18 hrs, then filtered to remove the solids. The filtrate was concentrated in vacuo to give an amber oil. MS (m/z): 169 (M+H)+; C9H13FN2 requir. 168.19 a chilled The reaction was then heated at reflux for 10 hrs filtered to remove the solids The filtrate was concentrated in vacuo to give an amber oil
来源 ID: ord-29fe5172f9d94884869e0ed43b282c11反应条件: temp:5.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-Amino-3-(2-fluorophenyl)propionamide was added carefully to a chilled (5°) mixture of LAH (1.0 g, 26.3 mmol) and 20 ml THF under argon. The reaction was then heated at reflux for 10 hrs. The reaction was cooled to 5° C. and carefully treated with Na2SO4.10 H2O. The resulting mixture was stirred for 18 hrs, then filtered to remove the solids. The filtrate was concentrated in vacuo to give an amber oil. MS (m/z): 169 (M+H)+; C9H13FN2 requir. 168.19 a chilled The reaction was then heated at reflux for 10 hrs filtered to remove the solids The filtrate was concentrated in vacuo to give an amber oil
来源 ID: ord-29fe5172f9d94884869e0ed43b282c11反应条件: temp:5.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-Amino-3-(2-fluorophenyl)propionamide was added carefully to a chilled (50°) mixture of LAH (1.0 g, 26.3 mmol) and 20 ml THF under argon. The reaction was then heated at reflux for 10 hrs. The reaction was cooled to 5° C. and carefully treated with Na2SO4.10H2O. The resulting mixture was stirred for 18 hrs, then filtered to remove the solids. The filtrate was concentrated in vacuo to give an amber oil. MS (m/z): 169 (M+H)+; C9H13FN2 requir. 168.19. a chilled The reaction was then heated at reflux for 10 hrs filtered to remove the solids The filtrate was concentrated in vacuo to give an amber oil
来源 ID: ord-7177bc8e9d6b4c96b1271afd6ee3f475反应条件: temp:5.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-Amino-3-(2-fluorophenyl)propionamide was added carefully to a chilled (5°) mixture of LAH (1.0 g, 26.3 mmol) and 20 ml THF under argon. The reaction was then heated at reflux for 10 hrs. The reaction was cooled to 5° C. and carefully treated with Na2SO4.10 H2O. The resulting mixture was stirred for 18 hrs, then filtered to remove the solids. The filtrate was concentrated in vacuo to give an amber oil. MS (m/z): 169 (M+H)+; C9H13FN2 requir. 168.19 a chilled The reaction was then heated at reflux for 10 hrs filtered to remove the solids The filtrate was concentrated in vacuo to give an amber oil
来源 ID: ord-9f6770dec1e143eaacef0b3e0e5b3803反应条件: temp:5.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-Amino-3-(2-fluorophenyl)propionamide was added carefully to a chilled (5°) mixture of LAH (1.0 g, 26.3 mmol) and 20 ml THF under argon. The reaction was then heated at reflux for 10 hrs. The reaction was cooled to 5° C. and carefully treated with Na2SO4.10 H2O. The resulting mixture was stirred for 18 hrs, then filtered to remove the solids. The filtrate was concentrated in vacuo to give an amber oil. MS (m/z): 169 (M+H)+; C9H13FN2 requir. 168.19 a chilled The reaction was then heated at reflux for 10 hrs filtered to remove the solids The filtrate was concentrated in vacuo to give an amber oil
来源 ID: ord-29fe5172f9d94884869e0ed43b282c11PubChem References
以下资料来自该化合物的公开数据库参考记录。
