反应 #4140946
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a1ba31acf9be40bfb015aaa2b5685b1f暂无可渲染的结构数据
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1-苯基-1,3-丁二酮(CAS 93-91-4)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a1ba31acf9be40bfb015aaa2b5685b1f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5a498399acb4443a944031cbd6ad587c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7fd19005d44440f78f29ce00a471b366反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-cb23385008ef4817927e576996635da5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-338657b08dcd439897de24d756c88afb反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d214aaea73d94cd58624909711f76a79反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A suspension of polymer-supported morpholine (Example 12), 1-phenyl-1,3-butanedione (81.5 mg, 0.5 mmol) and 4-carboxyphenyl hydrazine hydrochloride (113 mg, 0.6 mmol) in MeOH (2 mL) was shaken for 2.5 hours. The methanol was blown off under a stream of N2. DCM (4 mL) and polymer-supported isocyanate (Example 4A, 350 mg) were added and the reaction mixture shaken for 16 hours. An additional portion of polymer-supported isocyanate (120 mg) was added. After 4 hours the resin was filtered and washed with DCM (2×1.5 mL). The combined organic phases, when concentrated to dryness, gave 4-(3-methyl-5-phenyl-pyrazol-1-yl)-benzoic acid (67 mg, 48%), mp 159-162° C. Predicted mass for (C17H14N2O2+H)+, 278.1055. the reaction mixture shaken for 16 hours After 4 hours the resin was filtered washed with DCM (2×1.5 mL) The combined organic phases, when concentrated to dryness
来源 ID: ord-0a65c91df12f4451bfba0eff80a44bad反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2,-4-diethylthioxanthone 2-ethylanthraquinone; 2-methylanthraquinone; 1,8-dihydroxyanthraquinone; dibenzoylperoxide; 2,2-dimethoxy-2-phenylacetophenone; benzoin; 2-hydroxy-2-methylpropiophenone; benzaldehyde; 4-(2-hydroxyethoxy)phenyl-(2-hydroxy-2-methylpropyl)-ketone; benzoylacetone;
来源 ID: ord-d55c477e126d483aa6f3b23ac18c6b4f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 17.4 g of benzoylacetone in 100 ml of ethyl acetate is added a solution of 7.35 g of pyrrolidine in 50 ml of ethyl acetate. The reaction mixture is stirred at room temperature for 16 hours. The precipitated compound is collected by filtration to give 20.30 g of 3-(1-pyrrolidinyl)crotonophenone. The precipitated compound is collected by filtration
来源 ID: ord-d522da771bca4d258ebfce37ee653086反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1373963115d84d3593366cfe9aa36cee反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a1ba31acf9be40bfb015aaa2b5685b1f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a1ba31acf9be40bfb015aaa2b5685b1fPubChem References
以下资料来自该化合物的公开数据库参考记录。
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