反应 #4144276
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-47e48a5f649e4b6a8e2df219c158d307暂无可渲染的结构数据
CCOC(=O)C1CCC(=CC(=O)OC(C)(C)C)CC1中间体产品
ethyl 4-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethylidene]cyclohexane-1-carboxylate
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 | 乙基 4-[2-[(2-甲基丙-2-基)氧基]-2-氧代亚乙基]环己烷-1-羧酸乙酯 |
|---|---|
| English name | ethyl 4-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethylidene]cyclohexane-1-carboxylate |
| IUPAC 名称 | — |
| CAS号 | 218779-74-9 |
| 数据库编号 | 18340695 |
| 分子式 | — |
| 分子量 | — |
产品信息
乙基 4-[2-[(2-甲基丙-2-基)氧基]-2-氧代亚乙基]环己烷-1-羧酸乙酯(CAS 218779-74-9)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 18340695
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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-47e48a5f649e4b6a8e2df219c158d307反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of ethyl 4-(2-tert-butoxy-2-oxoethylidene)cyclohexanecarboxylate (5.3 g, 21 mmol) in CH2Cl2 (30 ml) was added TFA (30 ml). The solution was stirred at room temperature overnight. The solution was concentrated in vacuo to afford 6 g of product as colorless oil, which was used directly for next step without further purification. The solution was concentrated in vacuo
来源 ID: ord-541a1b14eb0c4ee9a88c94f95d40fa1f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of anhydrous lithium chloride (1.9 g, 45 mmol) in MeCN (100 ml) was added tert-butyl 2-(diethoxyphosphoryl)acetate (7.6 g, 30 mmol) at room temperature. The mixture was stirred for 30 min. TEA (6.4 ml, 45 mmol) was added and the mixture was stirred for another 30 min. Ethyl 4-oxocyclohexanecarboxylate (5.1 g, 30 mmol) was added and the mixture was stirred overnight. The precipitate was filtered off and the filtrate was concentrated to afford brown oil, which was purified by silica gel column (PE:EtOAc=10:1) to afford product (5 g, 62%). the mixture was stirred for another 30 min the mixture was stirred overnight The precipitate was filtered off the filtrate was concentrated to afford brown oil, which was purified by silica gel column (PE:EtOAc=10:1)
来源 ID: ord-128e909123a74c0092265e731240ebda反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-47e48a5f649e4b6a8e2df219c158d307反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-47e48a5f649e4b6a8e2df219c158d307反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of ethyl 4-(2-tert-butoxy-2-oxoethylidene)cyclohexanecarboxylate (5.3 g, 21 mmol) in CH2Cl2 (30 ml) was added TFA (30 ml). The solution was stirred at room temperature overnight. The solution was concentrated in vacuo to afford 6 g of product as colorless oil, which was used directly for next step without further purification. The solution was concentrated in vacuo
来源 ID: ord-bea00d74b052408f9587690813472c8b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of anhydrous lithium chloride (1.9 g, 45 mmol) in MeCN (100 ml) was added tert-butyl 2-(diethoxyphosphoryl)acetate (7.6 g, 30 mmol) at room temperature. The mixture was stirred for 30 min. TEA (6.4 ml, 45 mmol) was added and the mixture was stirred for another 30 min. Ethyl 4-oxocyclohexanecarboxylate (5.1 g, 30 mmol) was added and the mixture was stirred overnight. The precipitate was filtered off and the filtrate was concentrated to afford brown oil, which was purified by silica gel column (PE:EtOAc=10:1) to afford product (5 g, 62%). the mixture was stirred for another 30 min the mixture was stirred overnight The precipitate was filtered off the filtrate was concentrated to afford brown oil, which was purified by silica gel column (PE:EtOAc=10:1)
来源 ID: ord-d6bc09e0770f4cd694958a3123fba500反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of ethyl 4-(2-tert-butoxy-2-oxoethylidene)cyclohexanecarboxylate (5.3 g, 21 mmol) in CH2Cl2 (30 ml) was added TFA (30 ml). The solution was stirred at room temperature overnight. The solution was concentrated in vacuo to afford 6 g of product as colorless oil, which was used directly for next step without further purification. The solution was concentrated in vacuo
来源 ID: ord-541a1b14eb0c4ee9a88c94f95d40fa1f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of anhydrous lithium chloride (1.9 g, 45 mmol) in MeCN (100 ml) was added tert-butyl 2-(diethoxyphosphoryl)acetate (7.6 g, 30 mmol) at room temperature. The mixture was stirred for 30 min. TEA (6.4 ml, 45 mmol) was added and the mixture was stirred for another 30 min. Ethyl 4-oxocyclohexanecarboxylate (5.1 g, 30 mmol) was added and the mixture was stirred overnight. The precipitate was filtered off and the filtrate was concentrated to afford brown oil, which was purified by silica gel column (PE:EtOAc=10:1) to afford product (5 g, 62%). the mixture was stirred for another 30 min the mixture was stirred overnight The precipitate was filtered off the filtrate was concentrated to afford brown oil, which was purified by silica gel column (PE:EtOAc=10:1)
来源 ID: ord-128e909123a74c0092265e731240ebda反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a 250 mL round-bottom flask was charged ethyl 4-(2-tert-butoxy-2-oxoethylidene)cyclohexanecarboxylate (Int-4a, 5.38 g, 19.90 mmol) followed by EtOAc (100 mL). The flask was flushed with argon and then 5% palladium on carbon was added. The flask was sealed and degassed under vacuum. H2 (g) was added in a balloon and the reaction was allowed to stir 18 hours under hydrogen atmosphere. After 18 hours, the reaction mixture was filtered through celite. The solvent was removed in vacuo and the resulting oil was taken on without further purification. The flask was flushed with argon 5% palladium on carbon was added The flask was sealed degassed under vacuum H2 (g) was added in a balloon After 18 hours the reaction mixture was filtered through celite The solvent was removed in vacuo the resulting oil was taken on without further purification
来源 ID: ord-6fa096afaeb1418ea822e43253b338f9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of ethyl 4-(2-tert-butoxy-2-oxoethylidene)cyclohexanecarboxylate (5.3 g, 21 mmol) in CH2Cl2 (30 ml) was added TFA (30 ml). The solution was stirred at room temperature overnight. The solution was concentrated in vacuo to afford 6 g of product as colorless oil, which was used directly for next step without further purification. The solution was concentrated in vacuo
来源 ID: ord-bea00d74b052408f9587690813472c8b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of anhydrous lithium chloride (1.9 g, 45 mmol) in MeCN (100 ml) was added tert-butyl 2-(diethoxyphosphoryl)acetate (7.6 g, 30 mmol) at room temperature. The mixture was stirred for 30 min. TEA (6.4 ml, 45 mmol) was added and the mixture was stirred for another 30 min. Ethyl 4-oxocyclohexanecarboxylate (5.1 g, 30 mmol) was added and the mixture was stirred overnight. The precipitate was filtered off and the filtrate was concentrated to afford brown oil, which was purified by silica gel column (PE:EtOAc=10:1) to afford product (5 g, 62%). the mixture was stirred for another 30 min the mixture was stirred overnight The precipitate was filtered off the filtrate was concentrated to afford brown oil, which was purified by silica gel column (PE:EtOAc=10:1)
来源 ID: ord-d6bc09e0770f4cd694958a3123fba500PubChem References
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