反应 #4142594
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-609685e7a8b0439ab894bce341e5c0dc暂无可渲染的结构数据
CCNC1CCCCC1产品信息
<I>N</I>-乙基环己胺(CAS 5459-93-8)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 21609
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-609685e7a8b0439ab894bce341e5c0dc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d6c29dd7f1d14adb857fac791903cba4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-194c50e549c147328994feff75c18985反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7b321419d7b249e4ae94c1048ece264e反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-411e450ed7a941beb2196bc469229377反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5-Acetyl-2-acetamino-N-ethyl-N-cyclohexyl-benzylamine, m.p. 98-100° C was prepared from 5-acetyl-2-acetamino-benzyl bromide and N-ethyl-cyclohexylamine analogous to Example 8.
来源 ID: ord-98f066c78eba4715a367e64bbad94ccb反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-Amino-N-cyclohexyl-N-ethyl-5-methoxy-benzylamine was prepared from 2-amino-5-methoxy-benzyl alcohol, thionyl chlorie and N-ethyl-cyclohexylamine analogous to Example 1. Proof of structure by IR- and UV-spectra. IR-spectrum (methylenechloride): 3250 cm-1NH2 ; 3400 cm-1NH2 ; 2830 cm-1OCH3 ; 2800 cm-1N-ethyl (shoulder); 2850 cm-1 aliphatic hydrocarbon; 2930 cm-1 aliphatic hydrocarbon; 1500 cm-1C=C; 1600 cm-1C=C.
来源 ID: ord-2cde5289b1b2412795d4a76dc6a93da3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-609685e7a8b0439ab894bce341e5c0dc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-609685e7a8b0439ab894bce341e5c0dc反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-Cyclohexyl-N-ethyl 4-(1H-benzimidazylmethyl)benzamide was prepared by the method of Example 9 starting with N-ethylcyclohexylamine and reacting with trimethylaluminium and ethyl 4-(1H-benzimidazylmethyl)benzoate.
来源 ID: ord-7b6e96f13c034fbd87d1beac2e4792bc反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-Cyclohexyl-N-ethyl 4-(1H-benzimidazylmethyl)benzamide was prepared by the method of Example 9 starting with N-ethylcyclohexylamine and reacting with trimethylaluminium and ethyl 4-(1H-benzimidazylmethyl)benzoate.
来源 ID: ord-7b6e96f13c034fbd87d1beac2e4792bc反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5-(1-Cyclohexyl-1,2,3,4-tetrazol-5-yl)valeric acid (2.4 g) is dissolved in tetrahydrofuran (50 ml), and thereto is added triethylamine (1.1 g). To the mixture is added dropwise with stirring isobutyl chloroformate (1.5 g) under ice-cooling, and the mixture is stirred at room temperature for 30 minutes. To the mixture is added dropwise with stirring N-ethyl-cyclohexylamine (1.5 g) at room temperature, and the mixture is further stirred for 2 hours. After distilling off tetrahydrofuran, water is added to the residue, and the mixture is extracted with chloroform. The chloroform layer is washed with an aqueous saturated sodium chloride solution and dried over magnesium sulfate. Chloroform is distilled off, and the resulting residue is subjected to column chromatography (Kieselgel 60, made by Merck & Co., eluting solvent, chloroform) to isolate N-ethyl-N-cyclohexyl-5-(1-cyclohexyl-1,2,3,4-tetrazol-5-yl)valeramide (2.6 g), white crystalline powder (ether), m.p. 92°-95° C. cooling the mixture is further stirred for 2 hours After distilling off tetrahydrofuran, water is added to the residue the mixture is extracted with chloroform The chloroform layer is washed with an aqueous saturated sodium chloride solution dried over magnesium sulfate Chloroform is distilled off the resulting residue is subjected to column chromatography (Kieselgel 60, made by Merck & Co., eluting solvent, chloroform)
来源 ID: ord-31c072aa22fb4fdd875781c1ba6b6decPubChem References
以下资料来自该化合物的公开数据库参考记录。
