反应 #4162123
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-6742cb6789ea4c2a9c8a486c6e328e9b暂无可渲染的结构数据
CCOC1=CC=C(C=C1)Br产品信息
4-溴苯乙醚(CAS 588-96-5)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-6742cb6789ea4c2a9c8a486c6e328e9b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-acdc2fad2cbe4081be48ac9fabba9879反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-072aad9e8e174e6f99ce453791fb8511反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-73ade92cc9e24477be0ac55b523e5dd7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2b678553dd1c4db7860adafca4e113ba反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-559d10a270a645a0988990fe79a30857反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b1d81a648be04d2288250b7773699b57反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f0f3f473a4944c408ac2b7bf4f19a6fb反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-26c067681a9e40dd8815e7a4cb8ff7bf反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-593f271de0cb4470a901fddc22f2463e反应条件: temp:120.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 60 mg (0.23 mmol) N-Ethyl-2-(4-piperidin-4-yl-phenyl)-propionamide (VI.1) are added to a mixture of 46 mg (0.23 mmol) 1-bromo-4-ethoxy-benzene, 91 mg (97%, 0.92 mmol) sodium tert-butyrat, 28 mg (0.09 mmol) 2-(di-tert-butylphosphino)biphenyl and 21 mg (0.02 mmol) tris-(dibenzylidenaceton)-dipalladium(0) in 1.0 mL 1,4-dioxane. The mixture is stirred for 1.5 h at 120° C. in a microwave oven. After that time, the solvent is removed in vacuo and the residue is purified by HPLC (column: Waters XBridge 50; eluent A: water+0.3% NH4OH, eluent B: MeOH) to yield the desired product. After that time, the solvent is removed in vacuo the residue is purified by HPLC (column: Waters XBridge 50; eluent A: water+0.3% NH4OH, eluent B: MeOH)
来源 ID: ord-7a4590e1074647f39303c2a7adec6b9d反应条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 1.00 g (4.04 mmol) 2-(4-Piperidin-4-yl-phenyl)-propionic acid methyl ester (XI.3) are added to a mixture of 813 mg (4.04 mmol) 1-bromo-4-ethoxy-benzene, 1.60 g (97%, 16.2 mmol) sodium tert-butyrat, 483 mg (1.62 mmol) 2-(di-tert-butylphosphino)biphenyl and 370 mg (0.40 mmol) tris-(dibenzylidenaceton)-dipalladium(0) in 10 mL 1,4-dioxane. The mixture is stirred for 12 h at 70° C. After that time, the precipitate is filtered off and washed with ACN and diethyl ether. The residue is purified by HPLC (column: Waters XBridge 50; eluent A: water+0.3% NH4OH, eluent B: MeOH) to yield the desired product. After that time, the precipitate is filtered off washed with ACN and diethyl ether The residue is purified by HPLC (column: Waters XBridge 50; eluent A: water+0.3% NH4OH, eluent B: MeOH)
来源 ID: ord-231ffbaf321c48d4b9ccb408ca3d3bcfPubChem References
以下资料来自该化合物的公开数据库参考记录。
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