反应 #4146640
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-57aa4434bb72493da4a1636b7673ca63暂无可渲染的结构数据
CCCC(C1=CC=CC=C1)N产品信息
(1 -苯丁基)胺(CAS 2941-19-7)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-57aa4434bb72493da4a1636b7673ca63反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6d7cc9b10e2140dcb5bb424ad943ca3f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-cae6f0b1f52a45908a276195fbe9f9da反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared in a similar manner to example 4 using 4-methoxy-3-methyl-benzoic acid and 1-phenyl-butylamine. MS (M+H, 298.2).
来源 ID: ord-78c2e2ad4b854b0c96a5fb54b694f647反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-57aa4434bb72493da4a1636b7673ca63反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a degassed solution of 3,5-dibromopyridine (0.4 g, 1.7 mmol), sodium tert-butoxide (227 mg, 3.6 mmol), tris(dibenzylideneacetone)dipalladium (145 mg, 0.09 mmol) and rac-BINAP (105 mg, 0.2 mmol) in dry toluene (10 mL) was added 1-phenylbutan-1-amine (0.2 mL). The mixture was heated at reflux for 24 h and upon cooling to room temperature was diluted with ether and washed with brine (3×30 mL). The solution was dried (Na2SO4) and concentrated and the residue chromatographed using ethyl acetate-hexane (40:60) as eluant. From the early fractions 97 mg of pure product was obtained. The mixture was heated at reflux for 24 h washed with brine (3×30 mL) The solution was dried (Na2SO4) concentrated the residue chromatographed
来源 ID: ord-453eba706ba8470a87c049c94fe88b57反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a degassed solution of 3,5-dibromopyridine (0.4 g, 1.7 mmol), sodium tert-butoxide (227 mg, 3.6 mmol), tris(dibenzylideneacetone)dipalladium (145 mg, 0.09 mmol) and rac-BINAP (105 mg, 0.2 mmol) in dry toluene (10 mL) was added 1-phenylbutan-1-amine (0.2 mL). The mixture was heated at reflux for 24 h and upon cooling to room temperature was diluted with ether and washed with brine (3×30 mL). The solution was dried (Na2SO4) and concentrated and the residue chromatographed using ethyl acetate-hexane (40:60) as eluant. From the early fractions 97 mg of pure product was obtained. The mixture was heated at reflux for 24 h washed with brine (3×30 mL) The solution was dried (Na2SO4) concentrated the residue chromatographed
来源 ID: ord-453eba706ba8470a87c049c94fe88b57反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared in a similar manner to example 4 using 4-methoxy-3-methyl-benzoic acid and 1-phenyl-butylamine. MS (M+H, 298.2).
来源 ID: ord-78c2e2ad4b854b0c96a5fb54b694f647反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6d7cc9b10e2140dcb5bb424ad943ca3f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a degassed solution of 3,5-dibromopyridine (0.4 g, 1.7 mmol), sodium tert-butoxide (227 mg, 3.6 mmol), tris(dibenzylideneacetone)dipalladium (145 mg, 0.09 mmol) and rac-BINAP (105 mg, 0.2 mmol) in dry toluene (10 mL) was added 1-phenylbutan-1-amine (0.2 mL). The mixture was heated at reflux for 24 h and upon cooling to room temperature was diluted with ether and washed with brine (3×30 mL). The solution was dried (Na2SO4) and concentrated and the residue chromatographed using ethyl acetate-hexane (40:60) as eluant. From the early fractions 97 mg of pure product was obtained. The mixture was heated at reflux for 24 h washed with brine (3×30 mL) The solution was dried (Na2SO4) concentrated the residue chromatographed
来源 ID: ord-4c7be50b28a54697905b0b7f24a04384反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a degassed solution of 3,5-dibromopyridine (0.4 g, 1.7 mmol), sodium tert-butoxide (227 mg, 3.6 mmol), tris(dibenzylideneacetone)dipalladium (145 mg, 0.09 mmol) and rac-BINAP (105 mg, 0.2 mmol) in dry toluene (10 mL) was added 1-phenylbutan-1-amine (0.2 mL). The mixture was heated at reflux for 24 h and upon cooling to room temperature was diluted with ether and washed with brine (3×30 mL). The solution was dried (Na2SO4) and concentrated and the residue chromatographed using ethyl acetate-hexane (40:60) as eluant. From the early fractions 97 mg of pure product was obtained. The mixture was heated at reflux for 24 h washed with brine (3×30 mL) The solution was dried (Na2SO4) concentrated the residue chromatographed
来源 ID: ord-4c7be50b28a54697905b0b7f24a04384反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a degassed solution of 3,5-dibromopyridine (0.4 g, 1.7 mmol), sodium tert-butoxide (227 mg, 3.6 mmol), tris(dibenzylideneacetone)dipalladium (145 mg, 0.09 mmol) and rac-BINAP (105 mg, 0.2 mmol) in dry toluene (10 mL) was added 1-phenylbutan-1-amine (0.2 mL). The mixture was heated at reflux for 24 h and upon cooling to room temperature was diluted with ether and washed with brine (3×30 mL). The solution was dried (Na2SO4) and concentrated and the residue chromatographed using ethyl acetate-hexane (40:60) as eluant. From the early fractions 97 mg of pure product was obtained. The mixture was heated at reflux for 24 h washed with brine (3×30 mL) The solution was dried (Na2SO4) concentrated the residue chromatographed
来源 ID: ord-4c7be50b28a54697905b0b7f24a04384PubChem References
以下资料来自该化合物的公开数据库参考记录。
