反応 #4151485
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-258d77fa43f84decb4aa361749888951表示可能な構造データがありません
C1=CC=C(C=C1)C(=O)C2=CC=CC=C2N製品情報
(2-aminophenyl)-phenylmethanone (CAS 2835-77-0) 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 76080
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-258d77fa43f84decb4aa361749888951反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-3094772c35c84301bbe0a1f99678a703反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8a14a4f0bfc84b96bd3942bd4d91aaa8反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-1ffa4a54cc434603b8aa878bf811ecfe反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-3b4a641d35b7484eafdd5063b75a2731反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-96bb3a9e6aee422a96dc5df7d5919625反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 2-aminobenzophenone (100 g, 0.51 mol), urea (55 g, 0.93 mol) and acetic acid (300 mL) was stirred at 110° C. for 18 h. The reaction mixture was cooled to rt and filtered. The solid was washed with water and dried under reduced pressure. 4-Phenylquinazolin-2(1H)-one was isolated as a yellow solid and was used without further purification. filtered The solid was washed with water dried under reduced pressure
ソース ID: ord-fb37e12232134ee796b99af3643c1105反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-258d77fa43f84decb4aa361749888951反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 15.0 parts of 2-aminobenzophenone, 45 volume parts of acetic acid and 2 volume parts of concentrated hydrochloric acid, a solution of 5.6 parts of sodium nitrite in 16 volume parts of water is added dropwise under ice-cooling and stirring. The mixture is then added dropwise to a solution of 15.0 parts of ethyl β-chloroacetoacetate and 20 parts of potassium acetate in a mixture of 160 volume parts of ethanol and 35 volume parts of water. After 15 minutes precipitated crystals are collected to yield ethyl (2-benzoylphenyl)azochloroacetate as crystals. Recrystallization from ethanol gives yellow needles melting at 119°-120°C. cooling After 15 minutes precipitated crystals are collected
ソース ID: ord-f4a42234fbca45889650aba00849aa37反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 15.0 parts of 2-aminobenzophenone, 45 volume parts of acetic acid and 2 volume parts of concentrated hydrochloric acid, a solution of 5.6 parts of sodium nitrite in 16 volume parts of water is added dropwise under ice-cooling and stirring. The mixture is then added dropwise to a solution of 15.0 parts of ethyl β-chloroacetoacetate and 20 parts of potassium acetate in a mixture of 160 volume parts of ethanol and 35 volume parts of water. After 15 minutes precipitated crystals are collected to yield ethyl (2-benzoylphenyl)azochloroacetate as crystals. Recrystallization from ethanol gives yellow needles melting at 119°-120°C. cooling After 15 minutes precipitated crystals are collected
ソース ID: ord-f4a42234fbca45889650aba00849aa37反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: In the manner given in Preparation 1, 2-aminobenzophenone is refluxed with hydrazine hydrate in diethylene glycol to give 2-aminobenzophenone hydrazone.
ソース ID: ord-f82e5c9ebc424d78ab5b415009342efb反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: In the manner given in Preparation 1, 2-aminobenzophenone is refluxed with hydrazine hydrate in diethylene glycol to give 2-aminobenzophenone hydrazone.
ソース ID: ord-f82e5c9ebc424d78ab5b415009342efbPubChem 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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