反応 #4021274
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-85edac1ae734497298eef3cfe11665d4表示可能な構造データがありません
C(CCCCO)CCCN製品情報
8-aminooctan-1-ol (CAS 19008-71-0) 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 15919832
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
9 反応 · 9 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-85edac1ae734497298eef3cfe11665d4反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 8-Azido-octan-1-ol (1.99 g, 11.6 mmol) was dissolved in ethanol (25 mL) and Lindlar catalyst (200 mg) was added. The solution was hydrogenated at 50 psi, 30° C. for 2 hours. The catalyst was removed by filtration through Kieselguhr and the solvent was removed in vacuo to give a white solid 1.33 g (79% yield), mp 48°-53° C.; The catalyst was removed by filtration through Kieselguhr the solvent was removed in vacuo
ソース ID: ord-fd8c1ef75d4b4d6ba5b5d39f72ac4ac1反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 8-Azido-octan-1-ol (1.99 g, 11.6 mmol) was dissolved in ethanol (25 mL) and Lindlar catalyst (200 mg) was added. The solution was hydrogenated at 50 psi, 30° C. for 2 hours. The catalyst was removed by filtration through Kieselguhr and the solvent was removed in vacuo to give a white solid 1.33 g (79% yield), mp 48°-53° C.; The catalyst was removed by filtration through Kieselguhr the solvent was removed in vacuo
ソース ID: ord-2b16e87c22f24a0daa7f2da642e7c306反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 8-Azido-octan-1-ol (1.99 g, 11.6 mmol) was dissolved in ethanol (25 mL) and Lindlar catalyst (200 mg) was added. The solution was hydrogenated at 50 psi, 30° C. for 2 hours. The catalyst was removed by filtration through Kieselguhr and the solvent was removed in vacuo to give a white solid 1.33 g (79% yield), mp 48°-53° C.; The catalyst was removed by filtration through Kieselguhr the solvent was removed in vacuo
ソース ID: ord-2b16e87c22f24a0daa7f2da642e7c306反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-85edac1ae734497298eef3cfe11665d4反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: In an argon atmosphere, a mixture of methyl benzoate (3.0 mmol), 8-aminooctan-1-ol (3.6 mmol), Zn4(OCOCF3)6O (1.25 mol % in terms of mole number) and diisopropyl ether (5.0 ml) was heated to reflux for 20 hours, and as a result, 8-aminooctyl benzoate was obtained at a yield of 90%. The yield of 8-benzoylaminooctyl benzoate was 7%. was heated to reflux for 20 hours
ソース ID: ord-b2e89456cb7c4dc193f22164bc6d6734反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 8-Azido-octan-1-ol (1.99 g, 11.6 mmol) was dissolved in ethanol (25 mL) and Lindlar catalyst (200 mg) was added. The solution was hydrogenated at 50 psi, 30° C. for 2 hours. The catalyst was removed by filtration through Kieselguhr and the solvent was removed in vacuo to give a white solid 1.33 g (79% yield), mp 48°-53° C.; The catalyst was removed by filtration through Kieselguhr the solvent was removed in vacuo
ソース ID: ord-fd8c1ef75d4b4d6ba5b5d39f72ac4ac1反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 8-Azido-octan-1-ol (1.99 g, 11.6 mmol) was dissolved in ethanol (25 mL) and Lindlar catalyst (200 mg) was added. The solution was hydrogenated at 50 psi, 30° C. for 2 hours. The catalyst was removed by filtration through Kieselguhr and the solvent was removed in vacuo to give a white solid 1.33 g (79% yield), mp 48°-53° C.; The catalyst was removed by filtration through Kieselguhr the solvent was removed in vacuo
ソース ID: ord-2b16e87c22f24a0daa7f2da642e7c306反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-85edac1ae734497298eef3cfe11665d4PubChem 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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