反应 #4093324
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-b06e22e08c194b21ba217053207d5443暂无可渲染的结构数据
C1=CC=C(C=C1)NC(=O)NCCN产品信息
1-(2-氨基乙基)-3-苯基脲(CAS 53673-01-1)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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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b06e22e08c194b21ba217053207d5443反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-82e7c5476b6d4ad6a67e2b9e1acc864f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: When 3-chloropropanol is reacted with 1-(2-aminoethyl)-3-phenylurea and the resulting 1-[2-(3-hydroxypropylamino)ethyl]-3-phenylurea is reacted with diethyl carbonate according to the general processes of steps 1 and 2 of Example 2, there is obtained 1-[2-(tetrahydro-2-oxo-1,3-oxazin-3-yl)-ethyl]-3-phenylurea.
来源 ID: ord-1b721f344cc94762af0d011c54ff030d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: When 3-chloropropanol is reacted with 1-(2-aminoethyl)-3-phenylurea and the resulting 1-[2-(3-hydroxypropylamino)ethyl]-3-phenylurea is reacted with diethyl carbonate according to the general processes of steps 1 and 2 of Example 2, there is obtained 1-[2-(tetrahydro-2-oxo-1,3-oxazin-3-yl)-ethyl]-3-phenylurea.
来源 ID: ord-1b721f344cc94762af0d011c54ff030d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b06e22e08c194b21ba217053207d5443反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-82e7c5476b6d4ad6a67e2b9e1acc864f反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a stirring suspension of 0.057 mole of acetylethylene diamine in 100 ml of methylene chloride at 10° C. was added dropwise 0.057 mole of phenyl isocyanate. Soon after the addition a solid precipitated. 100 ml of anhydrous ether was added to the reaction mixture and stirring was continued for another 30 minutes. The solid was recovered by filtration, dissolved in 50 ml of 15% hydrochloric acid, and the solution was heated to 80° C. for 4 hours. Removal of the aqueous acid afforded the product which had a melting point of 190.4° C. Soon after the addition a solid precipitated 100 ml of anhydrous ether was added to the reaction mixture The solid was recovered by filtration dissolved in 50 ml of 15% hydrochloric acid Removal of the aqueous acid afforded the product which
来源 ID: ord-86a16948fe9f4a3c9bcc7449d8956d1a反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a stirring suspension of 0.057 mole of acetylethylene diamine in 100 ml of methylene chloride at 10° C. was added dropwise 0.057 mole of phenyl isocyanate. Soon after the addition a solid precipitated. 100 ml of anhydrous ether was added to the reaction mixture and stirring was continued for another 30 minutes. The solid was recovered by filtration, dissolved in 50 ml of 15% hydrochloric acid, and the solution was heated to 80° C. for 4 hours. Removal of the aqueous acid afforded the product which had a melting point of 190.4° C. Soon after the addition a solid precipitated 100 ml of anhydrous ether was added to the reaction mixture The solid was recovered by filtration dissolved in 50 ml of 15% hydrochloric acid Removal of the aqueous acid afforded the product which
来源 ID: ord-16af4a8882c64cf2be49768969f1b376反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a stirring suspension of 0.057 mole of acetylethylene diamine in 100 ml of methylene chloride at 10° C. was added dropwise 0.057 mole of phenyl isocyanate. Soon after the addition a solid precipitated. 100 ml of anhydrous ether was added to the reaction mixture and stirring was continued for another 30 minutes. The solid was recovered by filtration, dissolved in 50 ml of 15% hydrochloric acid, and the solution was heated to 80° C. for 4 hours. Removal of the aqueous acid afforded the product which had a melting point of 190.4° C. Soon after the addition a solid precipitated 100 ml of anhydrous ether was added to the reaction mixture The solid was recovered by filtration dissolved in 50 ml of 15% hydrochloric acid Removal of the aqueous acid afforded the product which
来源 ID: ord-c2049289a5504686876bdf79cc861b1c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: When 3-chloropropanol is reacted with 1-(2-aminoethyl)-3-phenylurea and the resulting 1-[2-(3-hydroxypropylamino)ethyl]-3-phenylurea is reacted with diethyl carbonate according to the general processes of steps 1 and 2 of Example 2, there is obtained 1-[2-(tetrahydro-2-oxo-1,3-oxazin-3-yl)ethyl]-3-phenylurea.
来源 ID: ord-870bed2442b84770973e9e0e0383bb67反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a stirring suspensions of 0.057 mole of acetylethylene diamine in 100 ml of methylene chloride at 10° C. was added dropwise 0.057 mole of phenyl isocyanate. Soon after the addition a solid precipitated. 100 ml of anhydrous ether was added to the reaction mixture and stirring was continued for another 30 minutes. The solid was recovered by filtration, dissolved in 50 ml of 15% hydrochloric acid, and the solution was heated to 80° C. for 4 hours. Removal of the aqueous acid afforded the product which had a melting point of 190.4° C. Soon after the addition a solid precipitated 100 ml of anhydrous ether was added to the reaction mixture The solid was recovered by filtration dissolved in 50 ml of 15% hydrochloric acid Removal of the aqueous acid afforded the product which
来源 ID: ord-db5d190a4bef463c9089748a2b8f9c6b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: When 3-chloropropanol is reacted with 1-(2-aminoethyl)-3-phenylurea and the resulting 1-[2-(3-hydroxypropylamino)ethyl]-3-phenylurea is reacted with diethyl carbonate according to the general processes of steps 1 and 2 of Example 2, there is obtained 1-[2-(tetrahydro-2-oxo-1,3-oxazin-3-yl)-ethyl]-3-phenylurea.
来源 ID: ord-1b721f344cc94762af0d011c54ff030dPubChem References
以下资料来自该化合物的公开数据库参考记录。
