反应 #3880274
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-5766db7cabed439db12b9dae541af067暂无可渲染的结构数据
CCCCC(=O)CC(=O)C(=O)OCC产品信息
乙基 2,4-二氧辛酸乙酯(CAS 102540-71-6)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 10998024
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
4 条反应 · 4 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5766db7cabed439db12b9dae541af067反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of sodium (9.3 g) in ethanol (200 ml) was added dropwise a mixture of diethyl oxalate (60 g) and 2-hexanone (40.9 g) with stirring. The reaction mixture was allowed to stand at room temperature for 45 hours. To a mixture of 1N-hydrochloric acid (500 ml) and hexane (500 ml) was added dropwise the reaction mixture with stirring vigorously. After the addition, water (500 ml) was added. The organic layer was washed with water (100 ml ×3), dried, and the solvent was removed by evaporation in vacuo. The residue was distilled under reduced pressure and the distillate at the boiling point of 110° to 111° C. (6 mmHg) was collected to give the desired product (57 g, 70%). was added dropwise the reaction mixture with stirring vigorously was added The organic layer was washed with water (100 ml ×3) dried the solvent was removed by evaporation in vacuo The residue was distilled under reduced pressure the distillate at the boiling point of 110° to 111° C. (6 mmHg) was collected
来源 ID: ord-d099c79ecfae426c80cf62a50effd09f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of ethyl oxalate (97.21 g) and hexan-2-one (66.58 g) was added dropwise to a solution of sodium ethoxide (50.1 g) in ethanol (160 ml) at reflux. The resultant mixture was heated at reflux for 2 h. The cooled reaction mixture was poured into a stirring mixture of ice (500 g) and water (100 ml) and the resultant slurry adjusted to pH 1.5(conc.H2SO4). The two layers were separated and the bottom layer extracted with toluene (2×200 ml). The combined organics were washed with brine (200 ml), dried and concentrated in vacuo to give a residue (107 g) which was purified by distillation to afford the title compound as a colourless liquid (67.2 g). at reflux at reflux for 2 h The cooled reaction mixture The two layers were separated the bottom layer extracted with toluene (2×200 ml) The combined organics were washed with brine (200 ml) dried concentrated in vacuo
来源 ID: ord-530407f4f3a24014934f7642abbc81ff反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To an ethanol (100 ml) solution of ethyl 2,4-dioxooctanoate (20 g) (K. Seki et al., Chem. Pharm. Bull., 32, 1568(1984)) was added, under ice-cooling, methoxyamine hydrochloride (8.4 g), and the mixture was stirred for one hour, then it was stirred for further 15 hours at room temperature. The reaction mixture was concentrated under reduced pressure, to which was added a saturated aqueous solution of sodium hydrogencarbonate, followed by extraction with ether. The extract solution was dried over anhydrous sodium sulfate, then the solvent was distilled off under reduced pressure. The residue was purified by column chromatography on silica gel to afford the title compound as a colorless oil (16.6 g, 72%). cooling The reaction mixture was concentrated under reduced pressure, to which was added a saturated aqueous solution of sodium hydrogencarbonate followed by extraction with ether The extract solution was dried over anhydrous sodium sulfate the solvent was distilled off under reduced pressure The residue was purified by column chromatography on silica gel
来源 ID: ord-dbca3273396c410ca29bbd87004d8f6aPubChem References
以下资料来自该化合物的公开数据库参考记录。
相关产品
12 related records
CAS 519164-14-8
CAS 36983-32-1
CAS 42564-36-3
CAS 64195-85-3
CAS 25007-54-9
CAS 861160-59-0
CAS 861351-52-2
CAS 33537-18-7
CAS 3682-42-6
CAS 74530-59-9
CAS 42212-75-9
CAS 152240-45-4
