反应 #4018853
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-c8002afb3b06404584f6de3e7f4af8aa暂无可渲染的结构数据
CCCCCCC(=O)CCC(=O)OC产品信息
4-氧代癸酸甲酯(CAS 7011-82-7)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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5 条反应 · 5 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c8002afb3b06404584f6de3e7f4af8aa反应条件: temp:25.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the resulting isobutyl 4-oxodecanoate were added 1 L of methanol and 250 g of 25% sodium hydroxide, and the mixture was stirred at 25° C. for 1 hour, followed by distilling off methanol in vacuo. Subsequently, thereto were added 2 L of water and 1 L of toluene. The resulting mixture was stirred at room temperature for 1 hour and then allowed to stand to separate the water phase. To the water phase were added 175 g of concentrated hydrochloric acid and 1.8 L of toluene. The resulting mixture was stirred for 10 minutes and then allowed to stand to separate the organic phase. Toluene in the organic phase was distilled off in vacuo and 1 L of toluene and 47.5 mL of concentrated sulfuric acid were added. The resulting mixture was heated under reflux for 1 hour and then cooled to 25° C. Thereto was gradually added 155 g of sodium hydrogencarbonate followed by stirring for 10 minutes at 25° C. Methanol was distilled off in vacuo and then 3 L of water and 1.8 L of toluene were added. The resulting mixture was stirred for 10 minutes at room temperature and then allowed to stand to separate the organic phase. Toluene in the organic phase was distilled off, yielding methyl 4-oxodecanoate (a compound in which R17 represents an n-pentyl group, and R18 represents a methyl group in the above formula (12)). Gas chromatographic analysis showed that the yield of methyl 4-oxodecanoate relative to isobutyl 4-oxodecanoate was 95%. by distilling off methanol in vacuo Subsequently, thereto were added 2 L of water and 1 L of toluene The resulting mixture was stirred at room temperature for 1 hour to separate the water phase To the water phase were added 175 g of concentrated hydrochloric acid and 1.8 L of toluene The resulting mixture was stirred for 10 minutes to separate the organic phase Toluene in the organic phase was distilled off in vacuo and 1 L of toluene and 47.5 mL of concentrated sulfuric acid were added The resulting mixture was heated under reflux for 1 hour cooled to 25° C by stirring for 10 minutes at 25° C Methanol was distilled off in vacuo 3 L of water and 1.8 L of toluene were added The resulting mixture was stirred for 10 minutes at room temperature to separate the organic phase Toluene in the organic phase was distilled off
来源 ID: ord-0535824467e640658d22b42a72a705c0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c8002afb3b06404584f6de3e7f4af8aa反应条件: temp:25.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the resulting isobutyl 4-oxodecanoate were added 1 L of methanol and 250 g of 25% sodium hydroxide, and the mixture was stirred at 25° C. for 1 hour, followed by distilling off methanol in vacuo. Subsequently, thereto were added 2 L of water and 1 L of toluene. The resulting mixture was stirred at room temperature for 1 hour and then allowed to stand to separate the water phase. To the water phase were added 175 g of concentrated hydrochloric acid and 1.8 L of toluene. The resulting mixture was stirred for 10 minutes and then allowed to stand to separate the organic phase. Toluene in the organic phase was distilled off in vacuo and 1 L of toluene and 47.5 mL of concentrated sulfuric acid were added. The resulting mixture was heated under reflux for 1 hour and then cooled to 25° C. Thereto was gradually added 155 g of sodium hydrogencarbonate followed by stirring for 10 minutes at 25° C. Methanol was distilled off in vacuo and then 3 L of water and 1.8 L of toluene were added. The resulting mixture was stirred for 10 minutes at room temperature and then allowed to stand to separate the organic phase. Toluene in the organic phase was distilled off, yielding methyl 4-oxodecanoate (a compound in which R17 represents an n-pentyl group, and R18 represents a methyl group in the above formula (12)). Gas chromatographic analysis showed that the yield of methyl 4-oxodecanoate relative to isobutyl 4-oxodecanoate was 95%. by distilling off methanol in vacuo Subsequently, thereto were added 2 L of water and 1 L of toluene The resulting mixture was stirred at room temperature for 1 hour to separate the water phase To the water phase were added 175 g of concentrated hydrochloric acid and 1.8 L of toluene The resulting mixture was stirred for 10 minutes to separate the organic phase Toluene in the organic phase was distilled off in vacuo and 1 L of toluene and 47.5 mL of concentrated sulfuric acid were added The resulting mixture was heated under reflux for 1 hour cooled to 25° C by stirring for 10 minutes at 25° C Methanol was distilled off in vacuo 3 L of water and 1.8 L of toluene were added The resulting mixture was stirred for 10 minutes at room temperature to separate the organic phase Toluene in the organic phase was distilled off
来源 ID: ord-0535824467e640658d22b42a72a705c0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c8002afb3b06404584f6de3e7f4af8aaPubChem 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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