反应 #4037657
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-89a1a53ea6344753835f5cd5cf30ff34暂无可渲染的结构数据
C1C2=C(C=CC=C2F)C(=O)CO1产品信息
8-氟异色满-4-酮(CAS 911825-99-5)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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8 条反应 · 8 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-89a1a53ea6344753835f5cd5cf30ff34反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was prepared from 8-fluoro-1H-isochromen-4(3H)-one via the procedure described above for the synthesis of 8-fluorochroman-4-amine.
来源 ID: ord-9f1552bc7a23457ea6cc169eb48adb84反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was prepared from 8-fluoro-1H-isochromen-4(3H)-one via the procedure described above for the synthesis of 8-fluorochroman-4-amine.
来源 ID: ord-9f1552bc7a23457ea6cc169eb48adb84反应条件: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 8-Fluoro-4-methylene-3,4-dihydro-1H-isochromene (400 mg) was dissolved in a solution of 1:1 MeOH/DCM (50 mL) and 1 mL of pyridine added. The mixture was chilled to −78° C. and ozone was bubbled through the mixture for 40 min. The reaction monitored by TLC. The mixture was purged with nitrogen at −78° C. for 10 min and then treated with PPh3. After concentration, the resulting residue was purified by preparative TLC to offer 300 mg of the title compound. added ozone was bubbled through the mixture for 40 min The mixture was purged with nitrogen at −78° C. for 10 min treated with PPh3 After concentration the resulting residue was purified by preparative TLC
来源 ID: ord-a1685c9202ae4a60957c272df3a05bd2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-89a1a53ea6344753835f5cd5cf30ff34反应条件: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 8-Fluoro-4-methylene-3,4-dihydro-1H-isochromene (400 mg) was dissolved in a solution of 1:1 MeOH/DCM (50 mL) and 1 mL of pyridine added. The mixture was chilled to −78° C. and ozone was bubbled through the mixture for 40 min. The reaction monitored by TLC. The mixture was purged with nitrogen at −78° C. for 10 min and then treated with PPh3. After concentration, the resulting residue was purified by preparative TLC to offer 300 mg of the title compound. added ozone was bubbled through the mixture for 40 min The mixture was purged with nitrogen at −78° C. for 10 min treated with PPh3 After concentration the resulting residue was purified by preparative TLC
来源 ID: ord-8f1c398c359b428d9bdb514bb3ab2a8e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was prepared from 8-fluoro-1H-isochromen-4(3H)-one via the procedure described above for the synthesis of 8-fluorochroman-4-amine.
来源 ID: ord-9f1552bc7a23457ea6cc169eb48adb84反应条件: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 8-Fluoro-4-methylene-3,4-dihydro-1H-isochromene (400 mg) was dissolved in a solution of 1:1 MeOH/DCM (50 mL) and 1 mL of pyridine added. The mixture was chilled to −78° C. and ozone was bubbled through the mixture for 40 min. The reaction monitored by TLC. The mixture was purged with nitrogen at −78° C. for 10 min and then treated with PPh3. After concentration, the resulting residue was purified by preparative TLC to offer 300 mg of the title compound. added ozone was bubbled through the mixture for 40 min The mixture was purged with nitrogen at −78° C. for 10 min treated with PPh3 After concentration the resulting residue was purified by preparative TLC
来源 ID: ord-a1685c9202ae4a60957c272df3a05bd2PubChem 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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