反応 #4151413
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-b30d959eff494194a79cf3e3724db25b表示可能な構造データがありません
CCCCCCC(=O)C製品情報
octan-2-one (CAS 111-13-7) 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 8093
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
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b30d959eff494194a79cf3e3724db25b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d35b4e9d75ab4e50bc9c3eabe8c4390b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-4e49f57fa416424ea1c63afb952521a3反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-84268149be224a3f9120f29a3b491a31反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-71124e0a28d845ce83fd4299afdb0e8c反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-def1fe9510314050b3a79bd113327ea6反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-439ede5c7d1d423893899da8bd0c1bab反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of octan-2-one (3.76 g, 0.29M) and hypophosphorus acid (91.5%, 2.09 g, 0.029M) is heated at 100° C. for 12 hours in the presence of Dowex 50W x 2 ion exchange resin (1 ml, aqueous slurry). The mixture is cooled to room temperature, methanol (50 ml) is added and the Dowex is removed by filtration. The filtrate is evaporated to an oily residue, which is dissolved in ethyl acetate, washed with water, brine, then dried (MgSO4). Removal of the solvent gives 1-hydroxy-1-methylheptylphosphonous acid. the Dowex is removed by filtration The filtrate is evaporated to an oily residue, which is dissolved in ethyl acetate washed with water, brine dried (MgSO4) Removal of the solvent
ソース ID: ord-3033695eda954703b461a84c97d44fcc反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A sample of the prepared hydroxy-ester pyrolyzes at 230° C. to a 1:1 mixture of 2-octanone and ethyl 3-methylvalerate.
ソース ID: ord-bb288b8954894c87b9a99acf8f62183a反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b30d959eff494194a79cf3e3724db25b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: g. 2,5-Dimethyl-3,6-diamyl-pyrazine was prepared by first forming 3-oximino-2-octanone by reacting 2-octanone with nitrosyl chloride according to the method of BOUVEAULT (loc.cit.). The autocondensation of two moles of the imino-ketone in the presence of zinc and acetic acid [according to the method described in Chimia 11, 310 (1957)] yielded 2,5-dimethyl-3,6-diamyl-pyrazine which had a b.p. of 78°C./0.03 mm. Hg.
ソース ID: ord-8295c367f56749868fe7aee80e82951b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: g. 2,5-Dimethyl-3,6-diamyl-pyrazine was prepared by first forming 3-oximino-2-octanone by reacting 2-octanone with nitrosyl chloride according to the method of BOUVEAULT (loc.cit.). The autocondensation of two moles of the imino-ketone in the presence of zinc and acetic acid [according to the method described in Chimia 11, 310 (1957)] yielded 2,5-dimethyl-3,6-diamyl-pyrazine which had a b.p. of 78°C./0.03 mm. Hg.
ソース ID: ord-8295c367f56749868fe7aee80e82951bPubChem 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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