反応 #4051811
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-66095e40e0184e0686e35dc03b96891b表示可能な構造データがありません
C1CN(CCN1)CC2=CC=C(C=C2)Br製品情報
1-[(4-bromophenyl)methyl]piperazine (CAS 91345-62-9) 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 876494
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
10 反応 · 10 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-66095e40e0184e0686e35dc03b96891b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-680f8eddd05c4cf8b96fb87113ef0a28反応条件: temp:120.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: This compound could be made in the following manner: 1-(4-Bromo-benzyl)-piperazine would be combined with 1 equ of 2-(Trifluoromethyl)phenyl boronic acid, 10 mol % of tetrakis(triphenylphosphine)palladium(0), 2M sodium carbonate solution, toluene and ethanol. The reaction mixture would be heated in a sealed tube at 120° C. overnight in an oil bath. The reaction mixture would then be filtered through Celite and concentrated in vacuo. The residue would then be purified by flash chromatography. The reaction mixture would then be filtered through Celite concentrated in vacuo The residue would then be purified by flash chromatography
ソース ID: ord-1fb88f186a634846804ef8ea61f4827c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: This compound could be made in the following manner: 2 g of 4-Bromobenzyl bromide and 1 equ. piperazine in acetonitrile would be stirred at room temperature and 1.1 g of potassium carbonate would be added. The reaction would be stirred at room temperature overnight. The solution would then be filtered through Celite and concentrated in vacuo to afford the crude product. Purification would be done by flash chromatography using a methylene chloride/methanol gradient. The reaction The solution would then be filtered through Celite concentrated in vacuo
ソース ID: ord-644b95f8f0c442a188f83b3f6390af57反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: This compound could be made in the following manner: 2 g of 4-Bromobenzyl bromide and 1 equ. piperazine in acetonitrile would be stirred at room temperature and 1.1 g of potassium carbonate would be added. The reaction would be stirred at room temperature overnight. The solution would then be filtered through Celite and concentrated in vacuo to afford the crude product. Purification would be done by flash chromatography using a methylene chloride/methanol gradient. The reaction The solution would then be filtered through Celite concentrated in vacuo
ソース ID: ord-644b95f8f0c442a188f83b3f6390af57反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-66095e40e0184e0686e35dc03b96891b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-680f8eddd05c4cf8b96fb87113ef0a28反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Synthesized according to General Procedure A: 4-bromobenzyl bromide (4{9}, 7 g, 28.0 mmol, 1 equiv.), piperazine (14.5 g, 168.0 mmol, 6 equiv.), THF (61.2 mL). Purification with flash column chromatography on silica gel (4:1 EtOAc:MeOH) afforded 5{9} (6.73 g, 94%) as a white solid. 1H-NMR (400 MHz, CDCl3): δ 7.42 (d, 2H, J=8.4 Hz) 7.19 (d, 2H, J=8.4 Hz), 3.42 (s, 2H) 2.87 (t, 4H, J=4.8 Hz), 2.38 (br s, 4H), 2.07 (br s, 1H). 13C-NMR (100 MHz, CDCl3): δ 137.1, 131.3, 130.9, 120.8, 62.8, 54.2, 45.9. Synthesized Purification with flash column chromatography on silica gel (4:1 EtOAc:MeOH) afforded 5{9} (6.73 g, 94%) as a white solid
ソース ID: ord-36fbd88bc78843baa2d93aa8c6aab1cc反応条件: temp:120.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: This compound could be made in the following manner: 1-(4-Bromo-benzyl)-piperazine would be combined with 1 equ of 2-(Trifluoromethyl)phenyl boronic acid, 10 mol % of tetrakis(triphenylphosphine)palladium(0), 2M sodium carbonate solution, toluene and ethanol. The reaction mixture would be heated in a sealed tube at 120° C. overnight in an oil bath. The reaction mixture would then be filtered through Celite and concentrated in vacuo. The residue would then be purified by flash chromatography. The reaction mixture would then be filtered through Celite concentrated in vacuo The residue would then be purified by flash chromatography
ソース ID: ord-1fb88f186a634846804ef8ea61f4827c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: This compound could be made in the following manner: 2 g of 4-Bromobenzyl bromide and 1 equ. piperazine in acetonitrile would be stirred at room temperature and 1.1 g of potassium carbonate would be added. The reaction would be stirred at room temperature overnight. The solution would then be filtered through Celite and concentrated in vacuo to afford the crude product. Purification would be done by flash chromatography using a methylene chloride/methanol gradient. The reaction The solution would then be filtered through Celite concentrated in vacuo
ソース ID: ord-644b95f8f0c442a188f83b3f6390af57PubChem 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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