反应 #4142120
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-41ce58d8cf4d40f79797d054c98d1dd7暂无可渲染的结构数据
C1=CC=C(C=C1)CNCCCCO产品信息
4-苯甲氨基-1-丁醇(CAS 59578-63-1)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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11 条反应 · 11 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-41ce58d8cf4d40f79797d054c98d1dd7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3c364ad305e94535a44da8d0c4d21e94反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-41ce58d8cf4d40f79797d054c98d1dd7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-41ce58d8cf4d40f79797d054c98d1dd7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Combine 4-amino-butan-1-ol (8.9 gm-0.1 mol), benzaldehyde (10.6 gm-0.1 mol), EtOH (100 ml) and PtO2 (0.3 gm), and hydrogenate the mixture at 45 lbs./sq.in. until H2 is no longer taken up. Filter, evaporate the solvent (in vacuo) to yield 17.7 gm of the desired compound. Rf is 0.70 (eluted from silica gel with 10% conc. NH3 /CH3OH). Filter evaporate the solvent (in vacuo)
来源 ID: ord-903fe23eb0b0453cbd0c0b252b58ca0a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3c364ad305e94535a44da8d0c4d21e94反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of [(4-tert-butyl-benzenesulfonyl)-p-tolyl-amino]-acetic acid with 4-benzylamino-butan-1-ol
来源 ID: ord-5f0f77b5e46949fa9dc9e51ca96f6f43反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Dissolve diaminooctane (10.8 g, 0.075) in methylene chloride (200 mL), methanol (100 mL) with di-t-butyldicarbonate (32.7 g, 0.156 mol). Stir the reaction overnight. Concentrate the reaction under vacuum and crystallize the residue from hexane to provide N, N'-bis(t-butoxycarbonyl)-1,8-octanediamine (20.2 g), mp 96-97° C. Combine 4-amino-butan-1-ol (8.9 g, 0.1 mol), benzaldehyde (10.6 g, 0.1 mol), ethanol (100 mL) and PtO2 (0.3 g) and hydrogenate at 45 lbs./sq. in. until hydrogen is no longer taken up. Filter the reaction and concentrate the filtrate under vacuum to provide 4-[[(phenyl)methyl]amino]-butan-1-ol (17.7 g), Rf =0.70 eluting with 10% conc. NH3 /methanol. Filter the reaction concentrate the filtrate under vacuum
来源 ID: ord-994281198ae34abeaf9ade1f582dd12c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Combine 4-amino-butan-1-o1 (8.9 gm - 0.1 mol), benzaldehyde (10.6 gm - 0.1 mol), EtOH (100 ml) and PtO2 (0.3 gm), and hydrogenate the mixture at 45 lbs./sq.in. until H2 is no longer taken up. Filter, evaporate the solvent (in vacuo) to yield 17.7 gm of the desired compound. Rf is 0.70 (eluted from silica gel with 10% conc. NH3 /CH3OH). Filter evaporate the solvent (in vacuo)
来源 ID: ord-c0823057e6a947a8809ee6f4dbcc46c9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Combine 4-amino-butan-1-ol (8.9 gm-0.1 mol), benzaldehyde (10.6 gm-0.1 mol), EtOH (100 ml) and PtO2 (0.3 gm), and hydrogenate the mixture at 45 lbs./sq.in. until H2 is no longer taken up. Filter, evaporate the solvent (in vacuo) to yield 17.7 gm of the desired compound. Rf is 0.70 (eluted from silica gel with 10% conc. NH3 /CH3OH). Filter evaporate the solvent (in vacuo)
来源 ID: ord-903fe23eb0b0453cbd0c0b252b58ca0a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3c364ad305e94535a44da8d0c4d21e94PubChem References
以下资料来自该化合物的公开数据库参考记录。
