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1H-Pyrrole, 2-phenyl-Appearance:detailed see specifications Storage:Keep away of light, cool place Package:25kg/drum;200kg/drum Application:It is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and
1H-Pyrrole, 2-phenyl- cas 3042-22-6Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
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2-phenyl-1H-PyrroleAppearance:white crystalline powder Storage:Shading, sealed, dry place. Package:aluminous bag Application:API Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(airport to airport) or by sea L
Quality assurance, stable process and affordable priceAppearance:detailed see specifications Storage:enquiry Package:according to the clients requirement Application:Pharmaceutical intermediates Transportation:Normal Port:chengdu
Stable supply of goods and provision of high-quality services Application:As raw materials in the field of medicine and biology
factory?direct?sale Application:Fine chemical intermediates, used as the main raw material for the synthesis of various pesticides, medicines, surfactants, polymer monomers, and antifungal agents
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Our mission is to provide high-quality and innovative products to our customers. By offering a broad range of products, custom synthesis and personalized services, Bide can help scientists speeding up their research in the chemical and pharmaceutical
(4-azidobut-1-yn-1-yl)benzene
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid; phenylmercuric acetate In nitromethane at 20℃; for 0.0833333h; Inert atmosphere; | 99% |
With 2,6-di-tert-butyl-4-methylpyridine; platinum(IV) chloride In ethanol for 6h; Heating; | 74% |
With silver hexafluoroantimonate; (bis(diphenylphosphino)methane)bis(chlorogold(I)) In dichloromethane at 35℃; Schmidt reaction; | 68% |
Conditions | Yield |
---|---|
With acetic acid In methanol at 20℃; for 2h; Inert atmosphere; Molecular sieve; | 99% |
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With zinc In ethanol for 16h; Inert atmosphere; Reflux; | 99% |
6-Phenoxy-3-phenyl-5,6-dihydro-4H-[1,2]oxazine
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With triiron dodecarbonyl In 1,2-dichloro-ethane at 80℃; for 20h; | 98% |
O-Vinylacetophenonoxime
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With potassium hydroxide; dimethyl sulfoxide at 95℃; for 1.33333h; | 96% |
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With sodium ethanolate In dimethyl sulfoxide at 100℃; for 24h; | 94% |
Conditions | Yield |
---|---|
With copper(l) iodide; sodium pentafluorophenolate In various solvent(s) at 130℃; for 12h; | 93% |
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With tris-(4,4’-di-tert-butyl-2,2’-bipyridine)ruthenium(II) hexafluorophosphate In chloroform at 20℃; for 3h; Concentration; Schlenk technique; Inert atmosphere; Irradiation; | 93% |
6-butoxy-3-phenyl-1,2-oxazine
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With triiron dodecarbonyl In 1,2-dichloro-ethane at 80℃; for 20h; | 91% |
pyrrole
iodobenzene
A
2-phenyl-1H-pyrrole
B
3-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
Stage #1: pyrrole With sodium hydride In tetrahydrofuran Stage #2: iodobenzene With zinc(II) chloride; johnphos; palladium diacetate In tetrahydrofuran at 100℃; for 21h; | A 91% B n/a |
With potassium tert-butylate In dimethyl sulfoxide at 80℃; for 22h; Sealed tube; Inert atmosphere; regioselective reaction; |
Conditions | Yield |
---|---|
With [10%-Pd/Al2O3] In 5,5-dimethyl-1,3-cyclohexadiene at 150℃; for 1.5h; Kinetics; Reagent/catalyst; Time; Concentration; Inert atmosphere; | A 90% B n/a |
With [10%-Pd/Al2O3] In 5,5-dimethyl-1,3-cyclohexadiene at 150℃; for 2h; | A 79% B n/a |
acetophenone O-vinyloxime
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With potassium tert-butylate In tert-butyl alcohol for 5h; Heating; | 89% |
Conditions | Yield |
---|---|
With palladium diacetate; magnesium oxide; triphenylphosphine In 1,4-dioxane at 150℃; | 86% |
With [Rh(coe)2Cl]2; tris(para-trifluoromethyl)phenyl phosphine In 1,4-dioxane at 120℃; | 78% |
With C52H44CoN4O4; potassium hydroxide; tert-butyl alcohol at 200℃; for 0.5h; Inert atmosphere; Darkness; regioselective reaction; | 69% |
iodobenzene
N-boc-2-pyrroleboronic acid
A
2-phenyl-1H-pyrrole
B
tert-butyl 2-phenyl-1H-pyrrole-1-carboxylate
Conditions | Yield |
---|---|
With methanol; tetrakis(triphenylphosphine) palladium(0); caesium carbonate In toluene for 24h; Suzuki coupling; Reflux; Inert atmosphere; | A 7% B 86% |
1-phenylbut-3-en-1-one acetyloxime
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With copper(I) bromide In toluene at 120℃; Solvent; Reagent/catalyst; Inert atmosphere; | 86% |
Dimethyl-(2-phenyl-pyrrol-1-yl)-amine
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With hydrogen; nickel In methanol; water under 3102.9 Torr; for 48h; Ambient temperature; | 85% |
2-phenyl-1-vinyl-1H-pyrrole
butan-1-ol
A
2-phenyl-1H-pyrrole
B
N-(α-butoxyethyl)-2-phenylpyrrole
Conditions | Yield |
---|---|
With ferric nitrate In water at 50℃; for 20h; Title compound not separated from byproducts; | A 10% B 85% |
With ferric nitrate In water at 50℃; for 20h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; | |
With ferric nitrate In water; butan-1-ol at 50℃; for 20h; Product distribution; | A 10 % Chromat. B 85 % Chromat. |
ferric nitrate In water at 50℃; for 20h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
C13H15NO2
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With copper(I) bromide In toluene at 120℃; Inert atmosphere; | 84% |
C15H19NO2
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With copper(I) bromide In toluene at 120℃; Inert atmosphere; | 82% |
(2E,4Z)-6-Azido-3-phenyl-hexa-2,4-dienoic acid ethyl ester
A
2-phenyl-1H-pyrrole
B
ethyl α-diazo-2-phenyl-2,5-dihydropyrrole-2-acetate
Conditions | Yield |
---|---|
With acetic acid In diethyl ether for 36h; Ambient temperature; | A 80% B n/a |
In benzene at 55℃; for 1.5h; | A n/a B 25% |
Conditions | Yield |
---|---|
Stage #1: trans-2-(tributylstannyl)-N,N-dibenzylcyclopropylamine; benzonitrile With n-butyllithium In tetrahydrofuran; hexane at -30 - 0℃; for 2.5h; Stage #2: With acetic acid In tetrahydrofuran; hexane | 80% |
1-phenylbut-3-en-1-one O-benzoyl oxime
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With copper(I) bromide In toluene at 120℃; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
With potassium hydroxide In dimethyl sulfoxide at 150℃; for 6h; | 79% |
With potassium hydroxide In dimethyl sulfoxide at 150℃; for 4h; | 44% |
Trofimov reaction; | |
In dimethyl sulfoxide Alkaline conditions; |
Conditions | Yield |
---|---|
With sodium hydroxide at 80℃; for 10h; under air; | 78% |
Inert atmosphere; Schlenk technique; | 74% |
With sodium hydroxide at 80℃; for 10h; Inert atmosphere; Schlenk technique; | 70% |
With sodium hydroxide at 80℃; Schlenk technique; Inert atmosphere; | 69% |
With palladium diacetate; acetic acid at 20℃; for 15h; |
Conditions | Yield |
---|---|
With sodium hydroxide at 80℃; for 10h; under air; regioselective reaction; | A 78% B n/a |
pyrrole
Diphenyliodonium triflate
A
2-phenyl-1H-pyrrole
B
iodobenzene
Conditions | Yield |
---|---|
With sodium hydroxide at 80℃; for 10h; under air; regioselective reaction; | A 78% B n/a |
pyrrole
diphenyliodonium bromide
A
2-phenyl-1H-pyrrole
B
iodobenzene
Conditions | Yield |
---|---|
With sodium hydroxide at 80℃; for 10h; under air; regioselective reaction; | A 77% B n/a |
2-bromo-pyrrole-1-carboxylic acid tert-butyl ester
phenylboronic acid
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
Stage #1: 2-bromo-pyrrole-1-carboxylic acid tert-butyl ester; phenylboronic acid With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate In ethanol; water; toluene at 110℃; for 12h; Sealed tube; Inert atmosphere; Stage #2: With potassium carbonate In methanol for 12h; Inert atmosphere; Reflux; | 77% |
2-phenyl-1H-pyrrole-4-carboxylic acid
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With ethanolamine for 2h; Heating; | 75% |
A
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran at 20℃; for 4h; Inert atmosphere; | A n/a B 75% |
Conditions | Yield |
---|---|
With C45H55O4P In dichloromethane at -65℃; for 12h; Inert atmosphere; enantioselective reaction; | 99% |
2-phenyl-1H-pyrrole
1-p-hydroxyphenyl-1-phenyl-1-ethanol
Conditions | Yield |
---|---|
With (11aS)-3,7-di-9-anthracenyl-10,11,12,13-tetrahydro-5-hydroxy-5-oxide diindeno[7,1de:10,70-fg][1,3,2] dioxaphosphocin In chloroform at 0 - 20℃; for 48h; Molecular sieve; enantioselective reaction; | 97% |
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With bismuth(lll) trifluoromethanesulfonate In dichloromethane at 20℃; for 0.0333333h; | 97% |
Conditions | Yield |
---|---|
With potassium hydroxide In dimethyl sulfoxide at 110℃; under 735.5 Torr; for 4.5h; Product distribution; different temperature and time; | 96% |
With potassium hydroxide In dimethyl sulfoxide at 120℃; under 735.5 Torr; for 6h; | 96% |
With potassium hydroxide In dimethyl sulfoxide at 100℃; Product distribution; various 2-, 2,3-, and 2,5-substituted pyrroles; various times; | |
With potassium hydroxide; benzophenone In dimethyl sulfoxide at 100℃; Product distribution; Mechanism; other pyrrole; other reagents; | |
With potassium hydroxide; t-butylnitrite at 20℃; Mechanism; other 2-arylpyrroles; other acetylenes; |
2-phenyl-1H-pyrrole
N,N-dimethyl-formamide
5-phenyl-1H-pyrrole-2-carbaldehyde
Conditions | Yield |
---|---|
Stage #1: 2-phenyl-1H-pyrrole; N,N-dimethyl-formamide With trichlorophosphate In toluene at 20℃; Vilsmeier-Haack Formylation; Cooling with ice; Inert atmosphere; Stage #2: With water; sodium hydrogencarbonate; sodium hydroxide In toluene at 0℃; for 3h; pH=7 - 12; Vilsmeier-Haack Formylation; Inert atmosphere; | 96% |
Stage #1: 2-phenyl-1H-pyrrole; N,N-dimethyl-formamide With trichlorophosphate at 0 - 40℃; for 1.16667h; Inert atmosphere; Stage #2: With water; sodium hydroxide for 0.5h; Reflux; | |
Stage #1: N,N-dimethyl-formamide With trichlorophosphate In dichloromethane for 0.0833333h; Vilsmeier-Haack Formylation; Inert atmosphere; Stage #2: 2-phenyl-1H-pyrrole In dichloromethane Vilsmeier-Haack Formylation; Inert atmosphere; Stage #3: With sodium hydroxide In tetrahydrofuran at 23℃; Vilsmeier-Haack Formylation; Inert atmosphere; regioselective reaction; | 139 mg |
2-phenyl-1H-pyrrole
1-(5-[1,1-biphenyl]-4-yl-1H-pyrrol-2-yl)-2,2,2-trifluoro-1-ethanol
2-[1,1-biphenyl]-4-yl-5-[2,2,2-trifluoro-1-(5-phenyl-1H-pyrrol-2-yl)-ethyl]-1H-pyrrole
Conditions | Yield |
---|---|
With phosphorus pentoxide In dichloromethane at 20℃; for 16h; Inert atmosphere; | 96% |
Conditions | Yield |
---|---|
Stage #1: 2-phenyl-1H-pyrrole; perfluorobenzaldehyde With trifluoroacetic acid In dichloromethane at 20℃; for 3h; Stage #2: With 2,3-dicyano-5,6-dichloro-p-benzoquinone In dichloromethane at 20℃; for 0.5h; Inert atmosphere; | 95% |
methyl-3-pyridylketone
2-phenyl-1H-pyrrole
diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
C17H18N2O
Conditions | Yield |
---|---|
With (11aR)-10,11,12,13-tetrahydro-5-hydroxy-3,7-bis[2,4,6-triisopropylphenyl]-5-oxide-diindeno[7,1-de:1',7’-fg][1,3,2]dioxaphosphocin In dichloromethane at 20℃; for 72h; Inert atmosphere; Schlenk technique; Molecular sieve; enantioselective reaction; | 94% |
Conditions | Yield |
---|---|
With phosphorus pentoxide In dichloromethane at 20℃; for 16h; | 94% |
2-phenyl-1H-pyrrole
2-chlorobenzalacetone
Conditions | Yield |
---|---|
With 9-amino-9-deoxy-epi-cinchonidine; trifluoroacetic acid In chlorobenzene at 20℃; for 24h; Michael Addition; enantioselective reaction; | 93% |
2-phenyl-1H-pyrrole
(4-bromophenyl)(pyridin-3-yl)methanone
diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
C22H19BrN2O
Conditions | Yield |
---|---|
With (11aR)-10,11,12,13-tetrahydro-5-hydroxy-3,7-bis[2,4,6-triisopropylphenyl]-5-oxide-diindeno[7,1-de:1',7’-fg][1,3,2]dioxaphosphocin In dichloromethane at 20℃; for 60h; Inert atmosphere; Schlenk technique; Molecular sieve; enantioselective reaction; | 93% |
2-phenyl-1H-pyrrole
3-(trifluoromethyl)-2H-benzo[b][1,4]oxazin-2-one
Conditions | Yield |
---|---|
With (11aR)-10,11,12,13-tetrahydro-5-hydroxy-3,7-bis[2,4,6-triisopropylphenyl]-5-oxide-diindeno[7,1-de:1',7’-fg][1,3,2]dioxaphosphocin In toluene at 20℃; for 12h; Friedel-Crafts Alkylation; enantioselective reaction; | 93% |
2-phenyl-1H-pyrrole
acridine hydrochloride
Conditions | Yield |
---|---|
With CdS/TiO2; oxygen In butan-1-ol at 20℃; for 5h; Irradiation; | 92% |
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With (R)-6,6'-bis(2,4,6-triisopropylphenyl)-1,1'-spirobiindanyl-7,7'-diyl hydrogen phosphate In toluene at 20℃; for 18h; Friedel-Crafts Alkylation; Inert atmosphere; enantioselective reaction; | 91% |
Conditions | Yield |
---|---|
With 2,2,2-trifluoroacetic acid ammonia In ethanol; water at 115℃; | 91% |
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With (R)-6,6'-bis(2,4,6-triisopropylphenyl)-1,1'-spirobiindanyl-7,7'-diyl hydrogen phosphate In toluene at 20℃; for 18h; Friedel-Crafts Alkylation; Inert atmosphere; enantioselective reaction; | 90% |
2-phenyl-1H-pyrrole
6-chloro-3-trifluoromethyl-benzoxazinone
Conditions | Yield |
---|---|
With (S)-3,3'-bis(2,4,6-tri-iso-propylphenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate In toluene at 20℃; for 18h; Friedel-Crafts Alkylation; Inert atmosphere; enantioselective reaction; | 90% |
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
Stage #1: 2-phenyl-1H-pyrrole With sodium hydride In N,N-dimethyl-formamide; paraffin oil at 25 - 28℃; for 0.5h; Stage #2: (E)-2-((6-chlorohex-2-en-1-yl)oxy)tetrahydro-2H-pyran In N,N-dimethyl-formamide; paraffin oil at 0 - 28℃; for 24h; | 90% |
2-phenyl-1H-pyrrole
Conditions | Yield |
---|---|
With bismuth(lll) trifluoromethanesulfonate In dichloromethane at 20℃; for 12h; | 90% |
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