反応 #3838457
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-d5fde7a9ba1948c7a4e60214eb06de03表示可能な構造データがありません
CC(=O)CCC1CCCC1製品情報
4-cyclopentylbutan-2-one (CAS 18216-75-6) 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 12427701
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
8 反応 · 8 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d5fde7a9ba1948c7a4e60214eb06de03反応条件: temp:-20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 10 parts of 3-cyclopentyl propionic acid are dissolved in 150 parts by volume of ethyl ether and chilled to -20° C. under argon. 50 parts by volume of 2.8 molar methyl magnesium bromide are added dropwise. After the addition of the methyl magnesium bromide is completed, the mixture is allowed to warm to room temperature. The cloudy reaction mixture is treated with 1N hydrochloric acid and the clearified reaction mixture is extracted with ether followed by ethyl acetate. The combined organic extracts are washed with water and saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered and the solvent evaporated under reduced pressure. The residual oil is chromatographed on silica gel using 10% ethyl acetate/hexane as the eluent, to provide 4-cyclopentyl-2-butanone. to warm to room temperature The cloudy reaction mixture the clearified reaction mixture is extracted with ether The combined organic extracts are washed with water and saturated sodium chloride solution dried over anhydrous sodium sulfate filtered the solvent evaporated under reduced pressure The residual oil is chromatographed on silica gel using 10% ethyl acetate/hexane as the eluent
ソース ID: ord-477d46f4e8b242e8b6ba3cdcf2761c43反応条件: temp:-20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 10 parts of 3-cyclopentyl propionic acid are dissolved in 150 parts by volume of ethyl ether and chilled to -20° C. under argon. 50 parts by volume of 2.8 molar methyl magnesium bromide are added dropwise. After the addition of the methyl magnesium bromide is completed, the mixture is allowed to warm to room temperature. The cloudy reaction mixture is treated with 1N hydrochloric acid and the clearified reaction mixture is extracted with ether followed by ethyl acetate. The combined organic extracts are washed with water and saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered and the solvent evaporated under reduced pressure. The residual oil is chromatographed on silica gel using 10% ethyl acetate/hexane as the eluent, to provide 4-cyclopentyl-2-butanone. to warm to room temperature The cloudy reaction mixture the clearified reaction mixture is extracted with ether The combined organic extracts are washed with water and saturated sodium chloride solution dried over anhydrous sodium sulfate filtered the solvent evaporated under reduced pressure The residual oil is chromatographed on silica gel using 10% ethyl acetate/hexane as the eluent
ソース ID: ord-6f79f686753c4eceb89340a9860a170d反応条件: temp:-20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 10 Parts of 3-cyclopentyl propionic acid are dissolved in 150 parts by volume of ethyl ether and chilled to -20° C. under argon. 50 Parts by volume of 2.8 molar methyl magnesium bromide are added dropwise. After the addition of the methyl magnesium bromide is completed, the mixture is allowed to warm to room temperature. The cloudy reaction mixture is treated with 1N hydrochloric acid and the clearified reaction mixture is extracted with ether followed by ethyl acetate. The combined organic extracts are washed with water and saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered and the solvent evaporated under reduced pressure. The residual oil is chromatographed on silica gel using 10% ethyl acetate/hexane as the eluent, to provide 4-cyclopentyl-2-butanone. to warm to room temperature The cloudy reaction mixture the clearified reaction mixture is extracted with ether The combined organic extracts are washed with water and saturated sodium chloride solution dried over anhydrous sodium sulfate filtered the solvent evaporated under reduced pressure The residual oil is chromatographed on silica gel using 10% ethyl acetate/hexane as the eluent
ソース ID: ord-059cd2243de54bd6b696ae6fdc329178反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d5fde7a9ba1948c7a4e60214eb06de03反応条件: temp:-20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 10 parts of 3-cyclopentyl propionic acid are dissolved in 150 parts by volume of ethyl ether and chilled to -20° C. under argon. 50 parts by volume of 2.8 molar methyl magnesium bromide are added dropwise. After the addition of the methyl magnesium bromide is completed, the mixture is allowed to warm to room temperature. The cloudy reaction mixture is treated with 1N hydrochloric acid and the clearified reaction mixture is extracted with ether followed by ethyl acetate. The combined organic extracts are washed with water and saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered and the solvent evaporated under reduced pressure. The residual oil is chromatographed on silica gel using 10% ethyl acetate/hexane as the eluent, to provide 4-cyclopentyl-2-butanone. to warm to room temperature The cloudy reaction mixture the clearified reaction mixture is extracted with ether The combined organic extracts are washed with water and saturated sodium chloride solution dried over anhydrous sodium sulfate filtered the solvent evaporated under reduced pressure The residual oil is chromatographed on silica gel using 10% ethyl acetate/hexane as the eluent
ソース ID: ord-477d46f4e8b242e8b6ba3cdcf2761c43反応条件: temp:-20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 10 parts of 3-cyclopentyl propionic acid are dissolved in 150 parts by volume of ethyl ether and chilled to -20° C. under argon. 50 parts by volume of 2.8 molar methyl magnesium bromide are added dropwise. After the addition of the methyl magnesium bromide is completed, the mixture is allowed to warm to room temperature. The cloudy reaction mixture is treated with 1N hydrochloric acid and the clearified reaction mixture is extracted with ether followed by ethyl acetate. The combined organic extracts are washed with water and saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered and the solvent evaporated under reduced pressure. The residual oil is chromatographed on silica gel using 10% ethyl acetate/hexane as the eluent, to provide 4-cyclopentyl-2-butanone. to warm to room temperature The cloudy reaction mixture the clearified reaction mixture is extracted with ether The combined organic extracts are washed with water and saturated sodium chloride solution dried over anhydrous sodium sulfate filtered the solvent evaporated under reduced pressure The residual oil is chromatographed on silica gel using 10% ethyl acetate/hexane as the eluent
ソース ID: ord-6f79f686753c4eceb89340a9860a170d反応条件: temp:-20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 10 Parts of 3-cyclopentyl propionic acid are dissolved in 150 parts by volume of ethyl ether and chilled to -20° C. under argon. 50 Parts by volume of 2.8 molar methyl magnesium bromide are added dropwise. After the addition of the methyl magnesium bromide is completed, the mixture is allowed to warm to room temperature. The cloudy reaction mixture is treated with 1N hydrochloric acid and the clearified reaction mixture is extracted with ether followed by ethyl acetate. The combined organic extracts are washed with water and saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered and the solvent evaporated under reduced pressure. The residual oil is chromatographed on silica gel using 10% ethyl acetate/hexane as the eluent, to provide 4-cyclopentyl-2-butanone. to warm to room temperature The cloudy reaction mixture the clearified reaction mixture is extracted with ether The combined organic extracts are washed with water and saturated sodium chloride solution dried over anhydrous sodium sulfate filtered the solvent evaporated under reduced pressure The residual oil is chromatographed on silica gel using 10% ethyl acetate/hexane as the eluent
ソース ID: ord-059cd2243de54bd6b696ae6fdc329178PubChem References
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