反应 #3884403
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-08f82eb71b0c4fdc9d4407d072493a91暂无可渲染的结构数据
CCN(CC)CCC(=O)OCC产品信息
乙醇合三氯乙醛(CAS 5515-83-3)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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7 条反应 · 7 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-08f82eb71b0c4fdc9d4407d072493a91反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The following materials were charged to the reaction vessel: anhydrous diethylamine (292 grams); ethyl acrylate (200 grams); phenothiazine (1.0 gram); and p-methoxyphenol (1.0 gram). This mixture was heated at reflux (about 56°-60°C.) for 24 hours. At the end of this period, unreacted amine was removed by distillation. The product was recovered at 80°-81°C. and 10 mm. mercury pressure in a yield of 96 percent. The product is designated herein as Amine Catalyst IX and has the formula, (C2H5)2N-CH2CH2 -C(O)OC2H5, as verified analytically by infrared spectroscopy. The following materials were charged to the reaction vessel This mixture was heated at reflux (about 56°-60°C.) for 24 hours At the end of this period, unreacted amine was removed by distillation The product was recovered at 80°-81°C.
来源 ID: ord-e2918e746ada44819f7c7e09103d3c33反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The following materials were charged to the reaction vessel: anhydrous diethylamine (292 grams); ethyl acrylate (200 grams); phenothiazine (1.0 gram); and p-methoxyphenol (1.0 gram). This mixture was heated at reflux (about 56°-60° C.) for 24 hours. At the end of this period, unreacted amine was removed by distillation. The product was recovered at 80°-81° C. and 10 mm. mercury pressure in a yield of 96 percent. The product is designated herein as Amine Catalyst IX and has the formula, (C2H5)2N-Ch2CH2 -C(O)OC2H5, as verified analytically by infrared spectroscopy. The following materials were charged to the reaction vessel This mixture was heated at reflux (about 56°-60° C.) for 24 hours At the end of this period, unreacted amine was removed by distillation The product was recovered at 80°-81° C.
来源 ID: ord-0d3bd8282d5f48509b07a5b3a3df3ed0反应条件: temp:58.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The following materials were charged to the reaction vessel: anhydrous diethylamine (292 grams); ethyl acrylate (200 grams); phenothiazine (1.0 gram); and p-methoxyphenol (1.0 gram). This mixture was heated at reflux (about 56-60° C.) for 24 hours. At the end of this period, unreacted amine was removed by distillation. The product was recovered at 80°-81° C. and 10 mm. mercury pressure in a yield of 96 percent. The product is designated herein as Amine Catalyst IX and has the formula, (C2H5)2N--CH2CH2 -C(O)OC2H5, as verified analytically by infrared spectroscopy. The following materials were charged to the reaction vessel This mixture was heated At the end of this period, unreacted amine was removed by distillation The product was recovered at 80°-81° C.
来源 ID: ord-bb017c5d72e947eb94998fa93856a5d1反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The following materials were charged to the reaction vessel: anhydrous diethylamine (292 grams); ethyl acrylate (200 grams); phenothiazine (1.0 gram); and p-methoxyphenol (1.0 gram). This mixture was heated at reflux (about 56°-60°C.) for 24 hours. At the end of this period, unreacted amine was removed by distillation. The product was recovered at 80°-81°C. and 10 mm. mercury pressure in a yield of 96 percent. The product is designated herein as Amine Catalyst IX and has the formula, (C2H5)2N-CH2CH2 -C(O)OC2H5, as verified analytically by infrared spectroscopy. The following materials were charged to the reaction vessel This mixture was heated at reflux (about 56°-60°C.) for 24 hours At the end of this period, unreacted amine was removed by distillation The product was recovered at 80°-81°C.
来源 ID: ord-e2918e746ada44819f7c7e09103d3c33反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The following materials were charged to the reaction vessel: anhydrous diethylamine (292 grams); ethyl acrylate (200 grams); phenothiazine (1.0 gram); and p-methoxyphenol (1.0 gram). This mixture was heated at reflux (about 56°-60° C.) for 24 hours. At the end of this period, unreacted amine was removed by distillation. The product was recovered at 80°-81° C. and 10 mm. mercury pressure in a yield of 96 percent. The product is designated herein as Amine Catalyst IX and has the formula, (C2H5)2N-Ch2CH2 -C(O)OC2H5, as verified analytically by infrared spectroscopy. The following materials were charged to the reaction vessel This mixture was heated at reflux (about 56°-60° C.) for 24 hours At the end of this period, unreacted amine was removed by distillation The product was recovered at 80°-81° C.
来源 ID: ord-0d3bd8282d5f48509b07a5b3a3df3ed0反应条件: temp:58.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The following materials were charged to the reaction vessel: anhydrous diethylamine (292 grams); ethyl acrylate (200 grams); phenothiazine (1.0 gram); and p-methoxyphenol (1.0 gram). This mixture was heated at reflux (about 56-60° C.) for 24 hours. At the end of this period, unreacted amine was removed by distillation. The product was recovered at 80°-81° C. and 10 mm. mercury pressure in a yield of 96 percent. The product is designated herein as Amine Catalyst IX and has the formula, (C2H5)2N--CH2CH2 -C(O)OC2H5, as verified analytically by infrared spectroscopy. The following materials were charged to the reaction vessel This mixture was heated At the end of this period, unreacted amine was removed by distillation The product was recovered at 80°-81° C.
来源 ID: ord-bb017c5d72e947eb94998fa93856a5d1PubChem References
以下资料来自该化合物的公开数据库参考记录。
