反应 #4116426
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-a43f29de73e74e5fb197c47e5e04de27暂无可渲染的结构数据
CCC(C)NCC1=CC=C(C=C1)Cl产品信息
CHEMBRDG-BB 4022328(CAS 46234-40-6)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-a43f29de73e74e5fb197c47e5e04de27反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-00b7726e4dfb4625b7f07f23a2d77e39反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 20 g of N-(4-chlorobenzyl)-N-sec.-butylamine were dissolved in 500 ml of ether. To the resulting solution, a solution of 14 g of phenyl isothiocyanate in 50 ml of ether was added dropwise, under cooling and stirring. After the dropwise addition, the temperature of the solution was gradually raised, and the solution was then stirred at room temperature for about 10 hours. The crystals which had been formed were separated by filtration. After recrystallization with a solvent mixture of hexane and ethyl alcohol, 30 g of N-(4-chlorobenzyl)-N-sec.-butyl-N'-phenylthiourea were obtained. Yield: 91%. Melting point: 134°-134.5° C. under cooling After the dropwise addition the temperature of the solution was gradually raised the solution was then stirred at room temperature for about 10 hours The crystals which had been formed were separated by filtration After recrystallization with a solvent mixture of hexane and ethyl alcohol
来源 ID: ord-8fee94989e1f483d8687b053b84066cc反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 20 g of N-(4-chlorobenzyl)-N-sec.-butylamine were dissolved in 500 ml of ether. To the resulting solution, a solution of 14 g of phenyl isothiocyanate in 50 ml of ether was added dropwise, under cooling and stirring. After the dropwise addition, the temperature of the solution was gradually raised, and the solution was then stirred at room temperature for about 10 hours. The crystals which had been formed were separated by filtration. After recrystallization with a solvent mixture of hexane and ethyl alcohol, 30 g of N-(4-chlorobenzyl)-N-sec.-butyl-N'-phenylthiourea were obtained. Yield: 91%. Melting point: 134°-134.5° C. under cooling After the dropwise addition the temperature of the solution was gradually raised the solution was then stirred at room temperature for about 10 hours The crystals which had been formed were separated by filtration After recrystallization with a solvent mixture of hexane and ethyl alcohol
来源 ID: ord-8fee94989e1f483d8687b053b84066cc反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 30 g (0.15 mole) of N-(4-chlorobenzyl)N-sec.-butylamine were dissolved in 500 ml of ether. To the resulting solution, a solution of 18 g (0.15 mole) of phenyl isocyanate in 50 ml of ether was added dropwise, under cooling and stirring. After the dropwise addition, the temperature of the solution was gradually raised, and the solution was then stirred at room temperature for about 10 hours. The crystals which had been formed were separated by filtration. After recrystallization with a solvent mixture of hexane and ethyl alcohol, 44 g of N-(4-chlorobenzyl)-N-sec.-butyl-N'-phenylurea were obtained. Yield: 93%. Melting point: 80°-81.5° C. under cooling After the dropwise addition the temperature of the solution was gradually raised the solution was then stirred at room temperature for about 10 hours The crystals which had been formed were separated by filtration After recrystallization with a solvent mixture of hexane and ethyl alcohol
来源 ID: ord-3b5ad136fafb44e4b42c8437085d5c4a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 30 g (0.15 mole) of N-(4-chlorobenzyl)N-sec.-butylamine were dissolved in 500 ml of ether. To the resulting solution, a solution of 18 g (0.15 mole) of phenyl isocyanate in 50 ml of ether was added dropwise, under cooling and stirring. After the dropwise addition, the temperature of the solution was gradually raised, and the solution was then stirred at room temperature for about 10 hours. The crystals which had been formed were separated by filtration. After recrystallization with a solvent mixture of hexane and ethyl alcohol, 44 g of N-(4-chlorobenzyl)-N-sec.-butyl-N'-phenylurea were obtained. Yield: 93%. Melting point: 80°-81.5° C. under cooling After the dropwise addition the temperature of the solution was gradually raised the solution was then stirred at room temperature for about 10 hours The crystals which had been formed were separated by filtration After recrystallization with a solvent mixture of hexane and ethyl alcohol
来源 ID: ord-3b5ad136fafb44e4b42c8437085d5c4a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 20 g of N-(4-chlorobenzyl)-N-sec.-butylamine were dissolved in 500 ml of ether. To the resulting solution, a solution of 14 g of phenyl isothiocyanate in 50 ml of ether was added dropwise, under cooling and stirring. After the dropwise addition, the temperature of the solution was gradually raised, and the solution was then stirred at room temperature for about 10 hours. The crystals which had been formed were separated by filtration. After recrystallization with a solvent mixture of hexane and ethyl alcohol, 30 g of N-(4-chlorobenzyl)-N-sec.-butyl-N'-phenylthiourea were obtained. Yield: 91%. Melting point: 134°-134.5° C. under cooling After the dropwise addition the temperature of the solution was gradually raised the solution was then stirred at room temperature for about 10 hours The crystals which had been formed were separated by filtration After recrystallization with a solvent mixture of hexane and ethyl alcohol
来源 ID: ord-8fee94989e1f483d8687b053b84066cc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a43f29de73e74e5fb197c47e5e04de27反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-00b7726e4dfb4625b7f07f23a2d77e39反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 30 g (0.15 mole) of N-(4-chlorobenzyl)N-sec.-butylamine were dissolved in 500 ml of ether. To the resulting solution, a solution of 18 g (0.15 mole) of phenyl isocyanate in 50 ml of ether was added dropwise, under cooling and stirring. After the dropwise addition, the temperature of the solution was gradually raised, and the solution was then stirred at room temperature for about 10 hours. The crystals which had been formed were separated by filtration. After recrystallization with a solvent mixture of hexane and ethyl alcohol, 44 g of N-(4-chlorobenzyl)-N-sec.-butyl-N'-phenylurea were obtained. Yield: 93%. Melting point: 80°-81.5° C. under cooling After the dropwise addition the temperature of the solution was gradually raised the solution was then stirred at room temperature for about 10 hours The crystals which had been formed were separated by filtration After recrystallization with a solvent mixture of hexane and ethyl alcohol
来源 ID: ord-3b5ad136fafb44e4b42c8437085d5c4a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 20 g of N-(4-chlorobenzyl)-N-sec.-butylamine were dissolved in 500 ml of ether. To the resulting solution, a solution of 14 g of phenyl isothiocyanate in 50 ml of ether was added dropwise, under cooling and stirring. After the dropwise addition, the temperature of the solution was gradually raised, and the solution was then stirred at room temperature for about 10 hours. The crystals which had been formed were separated by filtration. After recrystallization with a solvent mixture of hexane and ethyl alcohol, 30 g of N-(4-chlorobenzyl)-N-sec.-butyl-N'-phenylthiourea were obtained. Yield: 91%. Melting point: 134°-134.5° C. under cooling After the dropwise addition the temperature of the solution was gradually raised the solution was then stirred at room temperature for about 10 hours The crystals which had been formed were separated by filtration After recrystallization with a solvent mixture of hexane and ethyl alcohol
来源 ID: ord-8fee94989e1f483d8687b053b84066cc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-00b7726e4dfb4625b7f07f23a2d77e39PubChem References
以下资料来自该化合物的公开数据库参考记录。
