反应 #4047532
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-47c6d3faa68f4847a0b0bd40e2edf328暂无可渲染的结构数据
CCOC(=O)CCN(CC(=O)OCC)C(=O)OCC中间体产品
ethyl 3-[ethoxycarbonyl-(2-ethoxy-2-oxoethyl)amino]propanoate
结构、标识符和计算性质已按 CAS 与数据库记录完成匹配。
| 中文名称 | N-(乙氧羰基)-N-(2-乙氧基-2-氧代乙基)-Β-丙氨酸乙酯 |
|---|---|
| English name | ethyl 3-[ethoxycarbonyl-(2-ethoxy-2-oxoethyl)amino]propanoate |
| IUPAC 名称 | — |
| CAS号 | 14891-08-8 |
| 数据库编号 | 4381617 |
| 分子式 | — |
| 分子量 | — |
产品信息
N-(乙氧羰基)-N-(2-乙氧基-2-氧代乙基)-Β-丙氨酸乙酯(CAS 14891-08-8)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
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数据库编号 4381617
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合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-47c6d3faa68f4847a0b0bd40e2edf328反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 53.9 g of ethyl N-(ethoxycarbonylmethyl)-N-(ethoxycarbonyl)-β-alaninate in 200 ml of toluene is added dropwise to a stirred solution of potassium hexamethyldisilazide (429 ml, 0,653 M) in 125 ml of toluene under nitrogen and cooled to 0° . After 45 minutes at 0°, 21.6 ml of acetic acid is added followed by a solution of 100 g of sodium phosphate (monobasic) in 1 liter of water. The layers are separated, the organic layer is washed with pH 7 buffer, dried over sodium sulfate, filtered, concentrated and purified by flash chromatography using ethyl acetate/hexane (3:7) to yield ethyl 1-ethoxycarbonyl-3-oxo-pyrrolidine-2-carboxylate. cooled to 0° The layers are separated the organic layer is washed with pH 7 buffer dried over sodium sulfate filtered concentrated purified by flash chromatography
来源 ID: ord-e46a9b69046746968d35b8b36491fd6e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 49 g of ethyl N-(ethoxycarbonylmethyl)-β-alaninate and 30 ml of water cooled to -10° is added dropwise 27.6 ml of ethyl chloroformate followed by a solution of 12.7 g of sodium carbonate in 50 ml of water. The mixture is warmed to room temperature then heated at 55° for 50 minutes. The mixture is cooled, extracted with toluene, the extract is washed with 2N hydrochloric acid and water. The extract is dried over sodium sulfate, filtered, concentrated and distilled in vacuo to yield ethyl N-(ethoxycarbonylmethyl)-N-(ethoxycarbonyl)-β-alaninate. cooled to -10° then heated at 55° for 50 minutes The mixture is cooled extracted with toluene the extract is washed with 2N hydrochloric acid and water The extract is dried over sodium sulfate filtered concentrated distilled in vacuo
来源 ID: ord-0fffd0c3afab4ad6bf3f84d502264a7c反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Intermediate (e) (18.0 g, 65.2 mmol) was added to an ice bath cooled solution of NaOEt (32.6 mL) (21% by weight in EtOH) in absolute EtOH (41.7 mL) under a nitrogen atmosphere. The ice bath was removed and the mixture was heated at 80° C. for about 12 h until the condensation was complete as observed by TLC. The mixture was poured onto ice/water and extracted into EtOAc. The solvent was dried with Na2SO4, filtered, and evaporated to afford crude intermediate (f) as an off white solid (14.05 g) which was carried on without purification. The ice bath was removed The mixture was poured onto ice/water extracted into EtOAc The solvent was dried with Na2SO4 filtered evaporated
来源 ID: ord-cdf601ddefbc45f5a832363300a87067反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Intermediate (e) (18.0 g, 65.2 mmol) was added to an ice bath cooled solution of NaOEt (32.6 mL) (21% by weight in EtOH) in absolute EtOH (41.7 mL) under a nitrogen atmosphere. The ice bath was removed and the mixture was heated at 80° C. for about 12 h until the condensation was complete as observed by TLC. The mixture was poured onto ice/water and extracted into EtOAc. The solvent was dried with Na2SO4, filtered, and evaporated to afford crude intermediate (f) as an off white solid (14.05 g) which was carried on without purification. The ice bath was removed The mixture was poured onto ice/water extracted into EtOAc The solvent was dried with Na2SO4 filtered evaporated
来源 ID: ord-cdf601ddefbc45f5a832363300a87067反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Crude intermediate (c) (418 mmol) was dissolved in CH2Cl2 (275 mL) and triethylamine (58.3 mL, 418 mmol) was added followed by ethyl chloroformate (d) (39.8 mL, 418 mmol). The reaction was stirred at ambient temperature for about 24 h. After the reaction was complete, the volatile components were removed under vacuum. The crude product was then distilled under vacuum (about 5 mm Hg) and dissolved in EtOAc which was washed with aqueous saturated KHSO4×3, with brine×1 and dried over Na2SO4. Following filtration, the volatile components were removed under vacuum to afford intermediate (e) as a clear oil (74.8 g, 272 mmol) in 65% yield over two steps. the volatile components were removed under vacuum The crude product was then distilled under vacuum (about 5 mm Hg) dissolved in EtOAc which was washed with aqueous saturated KHSO4×3, with brine×1 dried over Na2SO4 filtration the volatile components were removed under vacuum
来源 ID: ord-458e5b3470394c35befca18d4ab875ad反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 53.9 g of ethyl N-(ethoxycarbonylmethyl)-N-(ethoxycarbonyl)-β-alaninate in 200 ml of toluene is added dropwise to a stirred solution of potassium hexamethyldisilazide (429 ml, 0,653 M) in 125 ml of toluene under nitrogen and cooled to 0° . After 45 minutes at 0°, 21.6 ml of acetic acid is added followed by a solution of 100 g of sodium phosphate (monobasic) in 1 liter of water. The layers are separated, the organic layer is washed with pH 7 buffer, dried over sodium sulfate, filtered, concentrated and purified by flash chromatography using ethyl acetate/hexane (3:7) to yield ethyl 1-ethoxycarbonyl-3-oxo-pyrrolidine-2-carboxylate. cooled to 0° The layers are separated the organic layer is washed with pH 7 buffer dried over sodium sulfate filtered concentrated purified by flash chromatography
来源 ID: ord-e46a9b69046746968d35b8b36491fd6e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 49 g of ethyl N-(ethoxycarbonylmethyl)-β-alaninate and 30 ml of water cooled to -10° is added dropwise 27.6 ml of ethyl chloroformate followed by a solution of 12.7 g of sodium carbonate in 50 ml of water. The mixture is warmed to room temperature then heated at 55° for 50 minutes. The mixture is cooled, extracted with toluene, the extract is washed with 2N hydrochloric acid and water. The extract is dried over sodium sulfate, filtered, concentrated and distilled in vacuo to yield ethyl N-(ethoxycarbonylmethyl)-N-(ethoxycarbonyl)-β-alaninate. cooled to -10° then heated at 55° for 50 minutes The mixture is cooled extracted with toluene the extract is washed with 2N hydrochloric acid and water The extract is dried over sodium sulfate filtered concentrated distilled in vacuo
来源 ID: ord-0fffd0c3afab4ad6bf3f84d502264a7c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 49 g of ethyl N-(ethoxycarbonylmethyl)-β-alaninate and 30 ml of water cooled to -10° is added dropwise 27.6 ml of ethyl chloroformate followed by a solution of 12.7 g of sodium carbonate in 50 ml of water. The mixture is warmed to room temperature then heated at 55° for 50 minutes. The mixture is cooled, extracted with toluene, the extract is washed with 2N hydrochloric acid and water. The extract is dried over sodium sulfate, filtered, concentrated and distilled in vacuo to yield ethyl N-(ethoxycarbonylmethyl)-N-(ethoxycarbonyl)-β-alaninate. cooled to -10° then heated at 55° for 50 minutes The mixture is cooled extracted with toluene the extract is washed with 2N hydrochloric acid and water The extract is dried over sodium sulfate filtered concentrated distilled in vacuo
来源 ID: ord-0fffd0c3afab4ad6bf3f84d502264a7c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-47c6d3faa68f4847a0b0bd40e2edf328反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 53.9 g of ethyl N-(ethoxycarbonylmethyl)-N-(ethoxycarbonyl)-β-alaninate in 200 ml of toluene is added dropwise to a stirred solution of potassium hexamethyldisilazide (429 ml, 0,653M) in 125 ml of toluene under nitrogen and cooled to 0°. After 45 minutes at 0°, 21.6 ml of acetic acid is added followed by a solution of 100 g of sodium phosphate (monobasic) in 1 liter of water. The layers are separated, the organic layer is washed with pH 7 buffer, dried over sodium sulfate, filtered, concentrated and purified by flash chromatography using ethyl acetate/hexane (3:7) to yield ethyl 1-ethoxycarbonyl-3-oxo-pyrrolidine-2-carboxylate. cooled to 0° The layers are separated the organic layer is washed with pH 7 buffer dried over sodium sulfate filtered concentrated purified by flash chromatography
来源 ID: ord-90e4bfde26964ddd89ed711af7ecc379反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a mixture of 49 g of ethyl N-(ethoxycarbonylmethyl)-β-alaninate and 30 ml of water cooled to -10° is added dropwise 27.6 ml of ethyl chloroformate followed by a solution of 12.7 g of sodium carbonate in 50 ml of water. The mixture is warmed to room temperature then heated at 55° for 50 minutes. The mixture is cooled, extracted with toluene, the extract is washed with 2N hydrochloric acid and water. The extract is dried over sodium sulfate, filtered, concentrated and distilled in vacuo to yield ethyl N-(ethoxycarbonylmethyl)-N-(ethoxycarbonyl)-β-alaninate. cooled to -10° then heated at 55° for 50 minutes The mixture is cooled extracted with toluene the extract is washed with 2N hydrochloric acid and water The extract is dried over sodium sulfate filtered concentrated distilled in vacuo
来源 ID: ord-b02302568f964419b62ac05ffbc53f1bPubChem References
以下资料来自该化合物的公开数据库参考记录。
