para-dichlorobenzene
benzoyl chloride
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
With sodium hydroxide; aluminium trichloride In water; toluene | 97% |
aluminium trichloride | 64% |
With aluminium trichloride at 150 - 170℃; |
Conditions | Yield |
---|---|
Stage #1: C15H21Cl2MgN With zinc(II) chloride In tetrahydrofuran at 0℃; for 0.166667h; Inert atmosphere; Stage #2: benzoyl chloride With tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran at 25℃; for 3h; Negishi Coupling; Inert atmosphere; | 97% |
(5-chloro-2-hydroxyphenyl)phenylmethanone
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
With phosphorus pentachloride Heating; | 78.4% |
Multi-step reaction with 4 steps 1: phosphorus oxychloride; 1,4-diazabicyclo[2.2.2]octane / benzene 2: phosphorus pentachloride / 3 h / 129 - 131 °C 3: 46 percent / 2 h / 245 °C View Scheme | |
Multi-step reaction with 4 steps 1: phosphorus oxychloride; 1,4-diazabicyclo[2.2.2]octane / benzene 2: 1,4-diazabicyclo[2.2.2]octane / benzene 3: phosphorus pentachloride / 2 h / 134 - 136 °C 4: 46 percent / 2 h / 245 °C View Scheme |
2,5-dichlorobenzoyl chloride
benzene
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
With aluminium trichloride In nitromethane at 20℃; for 24h; | 72% |
Stage #1: 2,5-dichlorobenzoyl chloride With iron(III) chloride In dichloromethane at 30℃; for 0.0833333h; Friedel-Crafts acylation; Microwave irradiation; Stage #2: benzene In dichloromethane at 70℃; for 0.25h; Friedel-Crafts acylation; Microwave irradiation; |
4-chloro-2-(α,α-dichlorobenzyl)phenyldiphenyl phosphate
A
(2,5-dichlorophenyl)(phenyl)methanone
B
chlorophosphoric acid diphenyl ester
Conditions | Yield |
---|---|
at 245℃; for 2h; | A 46% B n/a |
para-dichlorobenzene
benzoyl triflate
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
at 120℃; for 20h; | 25% |
4-chloro-2-(α,α-dichlorobenzyl)phenyl phosphochloridate
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
With trichlorophosphate under 1 Torr; Heating; | |
Multi-step reaction with 2 steps 1: 46 percent / 2 h / 245 °C View Scheme |
2-benzoyl-4-chlorophenylphosphorodichloridate
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: phosphorus pentachloride / 3 h / 129 - 131 °C 2: 46 percent / 2 h / 245 °C View Scheme | |
Multi-step reaction with 3 steps 1: 1,4-diazabicyclo[2.2.2]octane / benzene 2: phosphorus pentachloride / 2 h / 134 - 136 °C 3: 46 percent / 2 h / 245 °C View Scheme |
2-benzoyl-4-chlorophenyldiphenyl phosphate
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: phosphorus pentachloride / 2 h / 134 - 136 °C 2: 46 percent / 2 h / 245 °C View Scheme |
2,5-dichlorobenzoic acid
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: pyridine; 1,3,5-trichloro-2,4,6-triazine / dichloromethane / 0.25 h / 50 °C / Microwave irradiation 2.1: iron(III) chloride / dichloromethane / 0.08 h / 30 °C / Microwave irradiation 2.2: 0.25 h / 70 °C / Microwave irradiation View Scheme |
bromobenzene
2,5-dichloro-benzaldehyde
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: magnesium; iodine 1.2: -40 - 20 °C / Schlenk technique; Inert atmosphere 2.1: pyridinium chlorochromate / dichloromethane / 20 °C View Scheme |
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
With pyridinium chlorochromate In dichloromethane at 20℃; | |
With pyridinium chlorochromate In dichloromethane at 30℃; |
bromobenzene
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: magnesium; iodine / tetrahydrofuran / 20 °C / Reflux 1.2: 20 °C 2.1: pyridinium chlorochromate / dichloromethane / 30 °C View Scheme |
2,5-dichloro-benzaldehyde
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: magnesium; iodine / tetrahydrofuran / 20 °C / Reflux 1.2: 20 °C 2.1: pyridinium chlorochromate / dichloromethane / 30 °C View Scheme |
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
With C27H30Cl2CoN4; sodium triethylborohydride; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane In tetrahydrofuran at 20℃; for 18h; Schlenk technique; Inert atmosphere; enantioselective reaction; | 97% |
(2,5-dichlorophenyl)(phenyl)methanone
sodium phenylselenide
5-chloro-2-phenylselenobenzophenone
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 3h; Heating; | 93.7% |
(2,5-dichlorophenyl)(phenyl)methanone
1-aminoguanidine hydrochloride
C14H12Cl2N4*ClH
Conditions | Yield |
---|---|
With hydrogenchloride In ethanol; water for 5h; Heating; | 41% |
(2,5-dichlorophenyl)(phenyl)methanone
N-methyl-ethane-1,2-diamine
medazepam
Conditions | Yield |
---|---|
In acetonitrile for 24h; | 0.7% |
(2,5-dichlorophenyl)(phenyl)methanone
sodium methylate
Conditions | Yield |
---|---|
at 180℃; |
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
With methanol; sodium methylate |
(2,5-dichlorophenyl)(phenyl)methanone
tetrachloromethane
(2,5-dichlorophenyl)(phenyl)methanone
A
para-dichlorobenzene
B
benzoic acid
Conditions | Yield |
---|---|
at 200℃; |
(2,5-dichlorophenyl)(phenyl)methanone
2,5-dichlorobenzoic acid
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
With bis(triphenylphosphine)nickel(II) chloride; triphenylphosphine; zinc; [2,2]bipyridinyl In N,N-dimethyl acetamide at 60℃; for 24h; |
4-chloro-4'-isopropylbenzophenone
(2,5-dichlorophenyl)(phenyl)methanone
bis{4-(4-isopropylbenzoyl)phenyl}-terminated poly(benzophenone-2,5-diyl), product of nickel(0)-catalyzed polymerization; monomer(s): 4-chloro-4-isopropylbenzophenone; 2,5-dichlorobenzophenone
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; triphenylphosphine; zinc; nickel dichloride In N,N-dimethyl acetamide at 80℃; |
4-chloro-4'-isopropylbenzophenone
(2,5-dichlorophenyl)(phenyl)methanone
bis{4-(4-isopropylbenzoyl)phenyl}-terminated poly(benzophenone-2,5-diyl), product of nickel(0)-catalyzed polymerization, Mn 1.7E3 g/mol by GPC, PDI 1.7; monomer(s): 4-chloro-4-isopropylbenzophenone; 2,5-dichlorobenzophenone
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; triphenylphosphine; zinc; nickel dichloride In N,N-dimethyl acetamide at 80℃; |
4-chloro-4'-isopropylbenzophenone
(2,5-dichlorophenyl)(phenyl)methanone
bis{4-(4-isopropylbenzoyl)phenyl}-terminated poly(benzophenone-2,5-diyl), product of nickel(0)-catalyzed polymerization, Mn 2.4E3 g/mol by GPC, PDI 1.8; monomer(s): 4-chloro-4-isopropylbenzophenone; 2,5-dichlorobenzophenone
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; triphenylphosphine; zinc; nickel dichloride In N,N-dimethyl acetamide at 80℃; |
4-chloro-4'-isopropylbenzophenone
(2,5-dichlorophenyl)(phenyl)methanone
bis{4-(4-isopropylbenzoyl)phenyl}-terminated poly(benzophenone-2,5-diyl), product of nickel(0)-catalyzed polymerization, Mn 2.9E3 g/mol by GPC, PDI 2.1; monomer(s): 4-chloro-4-isopropylbenzophenone; 2,5-dichlorobenzophenone
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; triphenylphosphine; zinc; nickel dichloride In N,N-dimethyl acetamide at 80℃; |
4-chloro-4'-isopropylbenzophenone
(2,5-dichlorophenyl)(phenyl)methanone
bis{4-(4-isopropylbenzoyl)phenyl}-terminated poly(benzophenone-2,5-diyl), product of nickel(0)-catalyzed polymerization, Mn 3.3E3 g/mol by GPC, PDI 2.1; monomer(s): 4-chloro-4-isopropylbenzophenone; 2,5-dichlorobenzophenone
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; triphenylphosphine; zinc; nickel dichloride In N,N-dimethyl acetamide at 80℃; |
styrene
(2,5-dichlorophenyl)(phenyl)methanone
1-Chloro-4-(chloromethyl)benzene
polystyrene-block-poly(benzophenone-2,5-diyl)-block-polystyrene, Mn 3.25E4 g/mol by GPC, PDI 1.5, bimodal distribution; monomer(s): 4-chlorobenzyl chloride; 2,5-dichlorobenzophenone; styrene
Conditions | Yield |
---|---|
Stage #1: (2,5-dichlorophenyl)(phenyl)methanone; 1-Chloro-4-(chloromethyl)benzene With [2,2]bipyridinyl; triphenylphosphine; zinc; nickel dichloride In N,N-dimethyl acetamide at 80℃; Stage #2: styrene With copper(l) chloride; 4,4'-di-(5-nonyl)-2,2'-bipyridine In N,N-dimethyl acetamide at 110℃; for 48h; |
styrene
(2,5-dichlorophenyl)(phenyl)methanone
1-Chloro-4-(chloromethyl)benzene
polystyrene-block-poly(benzophenone-2,5-diyl)-block-polystyrene, Mn 1.157E5 g/mol by GPC, PDI 1.6, bimodal distribution; monomer(s): 4-chlorobenzyl chloride; 2,5-dichlorobenzophenone; styrene
Conditions | Yield |
---|---|
Stage #1: (2,5-dichlorophenyl)(phenyl)methanone; 1-Chloro-4-(chloromethyl)benzene With [2,2]bipyridinyl; triphenylphosphine; zinc; nickel dichloride In N,N-dimethyl acetamide at 80℃; Stage #2: styrene With copper(l) chloride; 4,4'-di-(5-nonyl)-2,2'-bipyridine In N,N-dimethyl acetamide at 110℃; for 48h; |
styrene
(2,5-dichlorophenyl)(phenyl)methanone
1-Chloro-4-(chloromethyl)benzene
polystyrene-block-poly(benzophenone-2,5-diyl)-block-polystyrene, Mn 1.001E5 g/mol by GPC, PDI 1.4, monomodal distribution; monomer(s): 4-chlorobenzyl chloride; 2,5-dichlorobenzophenone; styrene
Conditions | Yield |
---|---|
Stage #1: (2,5-dichlorophenyl)(phenyl)methanone; 1-Chloro-4-(chloromethyl)benzene With [2,2]bipyridinyl; triphenylphosphine; zinc; nickel dichloride In N,N-dimethyl acetamide at 80℃; Stage #2: styrene With copper(l) chloride; 4,4'-di-(5-nonyl)-2,2'-bipyridine In N,N-dimethyl acetamide at 110℃; for 48h; |
styrene
(2,5-dichlorophenyl)(phenyl)methanone
1-Chloro-4-(chloromethyl)benzene
polystyrene-block-poly(benzophenone-2,5-diyl)-block-polystyrene, Mn 8.59E4 g/mol by GPC, PDI 1.6, bimodal distribution; monomer(s): 4-chlorobenzyl chloride; 2,5-dichlorobenzophenone; styrene
Conditions | Yield |
---|---|
Stage #1: (2,5-dichlorophenyl)(phenyl)methanone; 1-Chloro-4-(chloromethyl)benzene With [2,2]bipyridinyl; triphenylphosphine; zinc; nickel dichloride In N,N-dimethyl acetamide at 80℃; Stage #2: styrene With copper(l) chloride; 4,4'-di-(5-nonyl)-2,2'-bipyridine In methoxybenzene at 110℃; for 14h; |
(2,5-dichlorophenyl)(phenyl)methanone
1-Chloro-4-(chloromethyl)benzene
poly(benzophenone-2,5-diyl), product of nickel(0)-catalyzed polymerization, molecular weight 3.1E3 g/mol by GPC, PDI 1.9; monomer(s): 4-chlorobenzyl chloride; 2,5-dichlorobenzophenone
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; triphenylphosphine; zinc; nickel dichloride In N,N-dimethyl acetamide at 80℃; |
(2,5-dichlorophenyl)(phenyl)methanone
1-Chloro-4-(chloromethyl)benzene
poly(benzophenone-2,5-diyl), product of nickel(0)-catalyzed polymerization, molecular weight 3.5E3 g/mol by GPC, PDI 2.1; monomer(s): 4-chlorobenzyl chloride; 2,5-dichlorobenzophenone
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; triphenylphosphine; zinc; nickel dichloride In N,N-dimethyl acetamide at 80℃; |
(2,5-dichlorophenyl)(phenyl)methanone
1-Chloro-4-(chloromethyl)benzene
poly(benzophenone-2,5-diyl), product of nickel(0)-catalyzed polymerization, molecular weight 3.9E3 g/mol by GPC, PDI 2.4; monomer(s): 4-chlorobenzyl chloride; 2,5-dichlorobenzophenone
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; triphenylphosphine; zinc; nickel dichloride In N,N-dimethyl acetamide at 80℃; |
(2,5-dichlorophenyl)(phenyl)methanone
Conditions | Yield |
---|---|
With sulfuric acid at 20 - 80℃; for 4h; |
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