反应 #4131081
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-c441211e90ab43f08f6ee655a58696b5暂无可渲染的结构数据
CC(=O)N1CCN(C1=O)C(=O)Cl产品信息
1-氯甲酰基-3-乙酰基环亚乙基脲(CAS 41730-71-6)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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8 条反应 · 8 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c441211e90ab43f08f6ee655a58696b5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c441211e90ab43f08f6ee655a58696b5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 20 parts by weight of N-acetyl-imidazolid-2-one mixed with 25 parts by weight of triethylamine and 150 parts by volume of dry benzene were first taken and 27 parts by weight of trimethylchlorosilane in 40 parts by volume of benzene were added dropwise at room temperature over the course of 30 minutes, with stirring. The mixture was subsequently boiled for 18 hours under reflux, moisture being excluded, and the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling and carefully rinsed with dry benzene. The benzene solution thus obtained was treated with a solution of 17 parts by weight of phosgene in 50 parts by volume of benzene at 5° C and left to stand overnight at 5° C. Thereafter the solvent was stripped off in vacuo and the residue was dried under an oil pump. It was recrystallized from acetone/pentane mixture. under reflux the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling carefully rinsed with dry benzene The benzene solution thus obtained left to stand overnight at 5° C the residue was dried under an oil pump It was recrystallized from acetone/pentane mixture
来源 ID: ord-7cc0f47e459d41969c9cc6c710a80aa9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 20 parts by weight of N-acetyl-imidazolid-2-one mixed with 25 parts by weight of triethylamine and 150 parts by volume of dry benzene were first taken and 27 parts by weight of trimethylchlorosilane in 40 parts by volume of benzene were added dropwise at room temperature over the course of 30 minutes, with stirring. The mixture was subsequently boiled for 18 hours under reflux, moisture being excluded, and the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling and carefully rinsed with dry benzene. The benzene solution thus obtained was treated with a solution of 17 parts by weight of phosgene in 50 parts by volume of benzene at 5° C and left to stand overnight at 5° C. Thereafter the solvent was stripped off in vacuo and the residue was dried under an oil pump. It was recrystallized from acetone/pentane mixture. under reflux the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling carefully rinsed with dry benzene The benzene solution thus obtained left to stand overnight at 5° C the residue was dried under an oil pump It was recrystallized from acetone/pentane mixture
来源 ID: ord-dcc99dd9767c4260ac1a098b451146e4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 20 parts by weight of N-acetyl-imidazolid-2-one mixed with 25 parts by weight of triethylamine and 150 parts by volume of dry benzene were first taken and 27 parts by weight of trimethylchlorosilane in 40 parts by volume of benzzene were added dropwise at room temperature over the course of 30 minutes, with stirring. The mixture was subsequently boiled for 18 hours under reflux, moisture being excluded, and the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling and carefully rinsed with dry benzene. The benzene solution thus obtained was treated with a solution of 17 parts by weight of phosgene in 50 parts by volume of benzene at 5° C and left to stand overnight at 5° C. Thereafter the solvent was stripped off in vacuo and the residue was dried under an oil pump. It was recrystallized from acetone/pentane mixture. under reflux the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling carefully rinsed with dry benzene The benzene solution thus obtained left to stand overnight at 5° C the residue was dried under an oil pump It was recrystallized from acetone/pentane mixture
来源 ID: ord-bf7d09f60ff14856b7d4f772a62e1452反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 20 parts by weight of N-acetyl-imidazolid-2-one mixed with 25 parts by weight of triethylamine and 150 parts by volume of dry benzene were first taken and 27 parts by weight of trimethylchlorosilane in 40 parts by volume of benzzene were added dropwise at room temperature over the course of 30 minutes, with stirring. The mixture was subsequently boiled for 18 hours under reflux, moisture being excluded, and the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling and carefully rinsed with dry benzene. The benzene solution thus obtained was treated with a solution of 17 parts by weight of phosgene in 50 parts by volume of benzene at 5° C and left to stand overnight at 5° C. Thereafter the solvent was stripped off in vacuo and the residue was dried under an oil pump. It was recrystallized from acetone/pentane mixture. under reflux the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling carefully rinsed with dry benzene The benzene solution thus obtained left to stand overnight at 5° C the residue was dried under an oil pump It was recrystallized from acetone/pentane mixture
来源 ID: ord-1bc95f9cfb2a4374a74ee2769aab3532反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 20 parts by weight of N-acetyl-imidazolid-2-one mixed with 25 parts by weight of triethylamine and 150 parts by volume of dry benzene were first taken and 27 parts by weight of trimethylchlorosilane in 40 parts by volume of benzene were added dropwise at room temperature over the course of 30 minutes, with stirring. The mixture was subsequently boiled for 18 hours under reflux, moisture being excluded, and the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling and carefully rinsed with dry benzene. The benzene solution thus obtained was treated with a solution of 17 parts by weight of phosgene in 50 parts by volume of benzene at 5° C and left to stand overnight at 5° C. Thereafter the solvent was stripped off in vacuo and the residue was dried under an oil pump. It was recrystallized from acetone/pentane mixture. under reflux the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling carefully rinsed with dry benzene The benzene solution thus obtained left to stand overnight at 5° C the residue was dried under an oil pump It was recrystallized from acetone/pentane mixture
来源 ID: ord-98e1a833e7934763b1d6567d499c4d74反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 20 parts by weight of N-acetyl-imidazolid-2-one mixed with 25 parts by weight of triethylamine and 150 parts by volume of dry benzene were first taken and 27 parts by weight of trimethylchlorosilane in 40 parts by volume of benzene were added dropwise at room temperature over the course of 30 minutes, with stirring. The mixture was subsequently boiled for 18 hours under reflux, moisture being excluded, and the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling and carefully rinsed with dry benzene. The benzene solution thus obtained was treated with a solution of 17 parts by weight of phosgene in 50 parts by volume of benzene at 5° C and left to stand overnight at 5° C. Thereafter the solvent was stripped off in vacuo and the residue was dried under an oil pump. It was recrystallized from acetone/pentane mixture. under reflux the triethylamine hydrochloride which precipitated (22 parts by weight = 100%) was filtered off after cooling carefully rinsed with dry benzene The benzene solution thus obtained left to stand overnight at 5° C the residue was dried under an oil pump It was recrystallized from acetone/pentane mixture
来源 ID: ord-3f501c2ce58d4a2c81760f79440b391bPubChem References
以下资料来自该化合物的公开数据库参考记录。
