反応 #3885925
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-21dbf5a15dc646ec8e5070121040cabf表示可能な構造データがありません
C1=C(C(=C(C(=C1F)Cl)Cl)Cl)C(=O)Cl製品情報
2,3,4-trichloro-5-fluorobenzoyl chloride (CAS 115549-05-8) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 14149869
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
11 反応 · 11 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-21dbf5a15dc646ec8e5070121040cabf反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b5e7d7b319534dcab15ae4a966672b2d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 480 g (1.83 mols) of 2,3,4-trichloro-5-fluorobenzoyl chloride are introduced, with 240 g (12 mols) of hydrogen fluoride, at -5° to 0° C. into a stirred autoclave fitted with a pressure-control valve, the apparatus is pressure-sealed and warmed to 70° C. in steps, corresponding to the evolution of HCl. The hydrogen chloride produced is continuously released at 4-5 bar. When the evolution of HCl is complete, the mixture is cooled, the excess pressure is released and the reaction mixture is fractionated. fitted with a pressure-control valve the apparatus is pressure-sealed
ソース ID: ord-21bf16f3a7db4138a26664dbdd4061e5反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 737 g (3.02 mols) of 2,3,4-trichloro-5-fluorobenzoic acid are introduced into 1.5 liters of thionyl chloride at room temperature, and the mixture is refluxed for 16 hours until the gas evolution ceases. Excess thionyl chloride is removed by distillation, and the residue is distilled. the mixture is refluxed for 16 hours until the gas evolution ceases Excess thionyl chloride is removed by distillation the residue is distilled
ソース ID: ord-3fbc7edb034d43bf846303d406b61176反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 737 g (3.02 mols) of 2,3,4-trichloro-5-fluorobenzoic acid are introduced into 1.5 liters of thionyl chloride at room temperature, and the mixture is refluxed for 16 hours until the gas evolution ceases. Excess thionyl chloride is removed by distillation, and the residue is distilled. the mixture is refluxed for 16 hours until the gas evolution ceases Excess thionyl chloride is removed by distillation the residue is distilled
ソース ID: ord-53b26ff73c864cbbada58d70898abcb7反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 737 g (3.02 mols) of 2,3,4-trichloro-5-fluorobenzoic acid are introduced into 1.5 liters of thionyl chloride at room temperature, and the mixture is refluxed for 16 hours until the gas evolution ceases. Excess thionyl chloride is removed by distillation, and the residue is distilled. the mixture is refluxed for 16 hours until the gas evolution ceases Excess thionyl chloride is removed by distillation the residue is distilled
ソース ID: ord-53b26ff73c864cbbada58d70898abcb7反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 480 g (1.83 mols) of 2,3,4-trichloro-5-fluorobenzoyl chloride are introduced, with 240 g (12 mols) of hydrogen fluoride, at -5° to 0° C. into a stirred autoclave fitted with a pressure-control valve, the apparatus is pressure-sealed and warmed to 70° C. in steps, corresponding to the evolution of HCl. The hydrogen chloride produced is continuously released at 4-5 bar. When the evolution of HCl is complete, the mixture is cooled, the excess pressure is released and the reaction mixture is fractionated. fitted with a pressure-control valve the apparatus is pressure-sealed
ソース ID: ord-21bf16f3a7db4138a26664dbdd4061e5反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 737 g (3.02 mols) of 2,3,4-trichloro-5-fluorobenzoic acid are introduced into 1.5 liters of thionyl chloride at room temperature, and the mixture is refluxed for 16 hours until the gas evolution ceases. Excess thionyl chloride is removed by distillation, and the residue is distilled. the mixture is refluxed for 16 hours until the gas evolution ceases Excess thionyl chloride is removed by distillation the residue is distilled
ソース ID: ord-3fbc7edb034d43bf846303d406b61176反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 737 g (3.02 mols) of 2,3,4-trichloro-5-fluorobenzoic acid are introduced into 1.5 liters of thionyl chloride at room temperature, and the mixture is refluxed for 16 hours until the gas evolution ceases. Excess thionyl chloride is removed by distillation, and the residue is distilled. the mixture is refluxed for 16 hours until the gas evolution ceases Excess thionyl chloride is removed by distillation the residue is distilled
ソース ID: ord-53b26ff73c864cbbada58d70898abcb7反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 480 g (1.83 mols) of 2,3,4-trichloro-5-fluorobenzoyl chloride are introduced, with 240 g (12 mols) of hydrogen fluoride, at -5° to 0° C. into a stirred autoclave fitted with a pressure-control valve, the apparatus is pressure-sealed and warmed to 70° C. in steps, corresponding to the evolution of HCl. The hydrogen chloride produced is continuously released at 4-5 bar. When the evolution of HCl is complete, the mixture is cooled, the excess pressure is released and the reaction mixture is fractionated. fitted with a pressure-control valve the apparatus is pressure-sealed
ソース ID: ord-21bf16f3a7db4138a26664dbdd4061e5反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 737 g (3.02 mols) of 2,3,4-trichloro-5-fluorobenzoic acid are introduced into 1.5 liters of thionyl chloride at room temperature, and the mixture is refluxed for 16 hours until the gas evolution ceases. Excess thionyl chloride is removed by distillation, and the residue is distilled. the mixture is refluxed for 16 hours until the gas evolution ceases Excess thionyl chloride is removed by distillation the residue is distilled
ソース ID: ord-3fbc7edb034d43bf846303d406b61176PubChem References
化合物の公開データベース記録に掲載された情報源です。
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