反应 #4153556
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-45e8aab36a68447290d75725f344d6f4暂无可渲染的结构数据
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3-乙氧基-4-羟基苯甲醛(CAS 121-32-4)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-45e8aab36a68447290d75725f344d6f4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c7c3bd3c71c044d1ba9b93a5044dbaf6反应条件: temp:0.00; pressure:0.00; stir:
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来源 ID: ord-4967db50c0e84ff0b8b1292bac58d8df反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8a8a6c15d38840eea4779c4781c1add3反应条件: temp:0.00; pressure:0.00; stir:
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来源 ID: ord-ac9624ca1f8e4504964a15b42a0e79ef反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2886a9067cac41ae87f723652c29d6c7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-087bbf4510924706b0aef654e928510f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2927df20863d4ddcbab4f0631f6253c0反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 11.8 g (46 mmol) of triethyl 2-phosphonobutyrate in 20 mL of tetrahydrofuran is added to a mixture of 1.8 g (46 mmol) of sodium hydride in 20 mL of tetrahydrofuran at 0° C. The reaction medium is stirred for 15 minutes. A solution of 3.4 g (20 mmol) of 3-ethoxy-4-hydroxybenzaldehyde prepared as in Example 32a in 20 mL of tetrahydrofuran is then added to the reaction mixture and the reaction medium is stirred at room temperature for 3 days. The reaction medium is then poured into saturated ammonium chloride solution, acidified with aqueous 2 N hydrochloric acid solution and extracted with ethyl acetate. The organic phases are combined, washed with water and dried over sodium sulfate. The solvent is evaporated off and the residue (12.5 g) is purified by chromatography on a column of silica eluted with an 80/20 heptane/ethyl acetate mixture. 3.7 g (71%) of ethyl 2-[1-(3-ethoxy-4-hydroxyphenyl)meth-(E)-ylidene]butyrate are obtained in the form of a yellow oil. is then added to the reaction mixture the reaction medium is stirred at room temperature for 3 days extracted with ethyl acetate washed with water dried over sodium sulfate The solvent is evaporated off the residue (12.5 g) is purified by chromatography on a column of silica eluted with an 80/20 heptane/ethyl acetate mixture
来源 ID: ord-a085885f2af64434acb1367abb06df80反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-hydroxy-3-methoxybenzaldehyde; 3,4-dimethoxybenzaldehyde heliotropin; 3,4-methylenedioxybenzaldehyde bourbonal; 3-ethoxy-4-hydroxybenzaldehyde; 3-hydroxy-4-methoxybenzaldehyde; 2-hydroxy-3-methoxybenzaldehyde; 2,5-dihydroxybenzaldehyde; and 2,4-diformyl-6-methoxyphenol.
来源 ID: ord-b726fc18e9004caf8052c3abab7cfd97PubChem References
以下资料来自该化合物的公开数据库参考记录。
