反応 #3884403
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-08f82eb71b0c4fdc9d4407d072493a91表示可能な構造データがありません
CCN(CC)CCC(=O)OCC製品情報
ethyl 3-(diethylamino)propanoate (CAS 5515-83-3) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 79649
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
7 反応 · 7 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-08f82eb71b0c4fdc9d4407d072493a91反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-e2918e746ada44819f7c7e09103d3c33反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-0d3bd8282d5f48509b07a5b3a3df3ed0反応条件: temp:58.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-bb017c5d72e947eb94998fa93856a5d1反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-e2918e746ada44819f7c7e09103d3c33反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-0d3bd8282d5f48509b07a5b3a3df3ed0反応条件: temp:58.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-bb017c5d72e947eb94998fa93856a5d1PubChem References
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