反応 #4162123
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-6742cb6789ea4c2a9c8a486c6e328e9b表示可能な構造データがありません
CCOC1=CC=C(C=C1)Br製品情報
1-bromo-4-ethoxybenzene (CAS 588-96-5) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 68523
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-6742cb6789ea4c2a9c8a486c6e328e9b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-acdc2fad2cbe4081be48ac9fabba9879反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-072aad9e8e174e6f99ce453791fb8511反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-73ade92cc9e24477be0ac55b523e5dd7反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-2b678553dd1c4db7860adafca4e113ba反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-559d10a270a645a0988990fe79a30857反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b1d81a648be04d2288250b7773699b57反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f0f3f473a4944c408ac2b7bf4f19a6fb反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-26c067681a9e40dd8815e7a4cb8ff7bf反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-593f271de0cb4470a901fddc22f2463e反応条件: temp:120.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-7a4590e1074647f39303c2a7adec6b9d反応条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-231ffbaf321c48d4b9ccb408ca3d3bcfPubChem References
化合物の公開データベース記録に掲載された情報源です。
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