反应 #4121268
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-837b857b5fe34d0fa1e8d7a2ec9d85b0暂无可渲染的结构数据
CC(=O)CCC1=CC(=CC=C1)F产品信息
4-(3-氟苯基)丁烷-2-酮(CAS 3506-77-2)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
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-837b857b5fe34d0fa1e8d7a2ec9d85b0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e9721be9631948c08ffd60ab5756ec3d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b9ac25e43ab24d818c0fbd98af89ce61反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-837b857b5fe34d0fa1e8d7a2ec9d85b0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e9721be9631948c08ffd60ab5756ec3d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: In accordance with the same procedures as in Step 2 of Preparation 1, except for using 4-hydrazino-1H-pyridin-2-one (5.39 g, 43.1 mmol) prepared in Step 1 of Preparation 1 and 3-fluorobenzylacetone (9.82 ml, 65.1 mmol), the titled compound was obtained as a white solid. (Yield: 63.4%) The product was used in the subsequent reaction without further purification. In accordance with the same procedures as in Step 2 of Preparation 1
来源 ID: ord-a84cd9789cab48c49994923261d5e840反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: In accordance with the same procedures as in Step 2 of Preparation 1, except for using 4-hydrazino-1H-pyridin-2-one (5.39 g, 43.1 mmol) prepared in Step 1 of Preparation 1 and 3-fluorobenzylacetone (9.82 ml, 65.1 mmol), the titled compound was obtained as a white solid. (Yield: 63.4%) The product was used in the subsequent reaction without further purification. In accordance with the same procedures as in Step 2 of Preparation 1
来源 ID: ord-309c57b3ae75447b86efa4ae24b5c076反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared according to the procedure described in Example 24, Step 1, using 5-(4-bromo-phenyl)-3-methyl-isoxazol-4-ylamine and 4-(3-fluoro-phenyl)-butan-2-one. Prepared
来源 ID: ord-47cf4f7a41164546850a9f866628851b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared according to the procedure described in Example 24, Step 1, using 1-[4′-(4-amino-3-methyl-isoxazol-5-yl)-biphenyl-4-yl]-cyclopropanecarboxylic acid ethyl ester and 4-(3-fluoro-phenyl)-butan-2-one. Prepared
来源 ID: ord-f128822cdb5b4e3aa36319a9c426f94e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared according to the procedure described in Example 8, Step 1, using 5-(4-bromo-phenyl)-3-methyl-isoxazol-4-ylamine and 4-(3-fluoro-phenyl)-butan-2-one. Prepared
来源 ID: ord-08b820c55918450c8a340578b1b26740反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared according to the procedure described in Example 8, Step 1, using 1-[4′-(4-amino-3-methyl-isoxazol-5-yl)-biphenyl-4-yl]-cyclopropanecarboxylic acid ethyl ester and 4-(3-fluoro-phenyl)-butan-2-one. Prepared
来源 ID: ord-59c35fadc8334d4da456e722f2d41f99反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e9721be9631948c08ffd60ab5756ec3dPubChem References
以下资料来自该化合物的公开数据库参考记录。
