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inquirymethyl 4-chloro-indole-1-carboxylate
4-chloro-1H-indole
Conditions | Yield |
---|---|
With potassium hydroxide In methanol for 1h; Reflux; | 99% |
With sodium hydroxide In methanol for 0.25h; Heating; | 79% |
2-(2-amino-6-chlorophenyl)ethyl alcohol
4-chloro-1H-indole
Conditions | Yield |
---|---|
tris(triphenylphosphine)ruthenium(II) chloride In toluene for 6h; Heating; | 92% |
tris(triphenylphosphine)ruthenium(II) chloride In toluene for 6h; Rate constant; Heating; | 92% |
tris(triphenylphosphine)ruthenium(II) chloride In toluene Heating; | 80% |
2-(2-chloro-6-nitrophenyl)-ethanol
4-chloro-1H-indole
Conditions | Yield |
---|---|
With hydrogen In o-xylene under 760.051 Torr; for 12h; Reflux; | 75% |
Multi-step reaction with 2 steps 1: H2 / 5percent Pd-C / ethyl acetate 2: 80 percent / RuCl2(PPh3)3 / toluene / Heating View Scheme | |
Multi-step reaction with 2 steps 1: 45 percent / Zn/CaCl2/H2O / ethanol / 8 h / Heating 2: 92 percent / RuCl2(PPh3)3 / toluene / 6 h / Heating View Scheme | |
Multi-step reaction with 6 steps 1: triethylamine / dichloromethane / 0 - 25 °C 2: 1,4-diaza-bicyclo[2.2.2]octane / N,N-dimethyl acetamide / 12 h / 75 °C 3: zinc; acetic acid / 24 h / 70 °C 4: pyridine / dichloromethane / 0 - 25 °C 5: bis(benzonitrile)palladium(II) dichloride; tert.-butylnitrite; oxygen / tert-butyl alcohol / 16 h / 70 °C / 760.05 Torr / Schlenk technique 6: potassium hydroxide / methanol / 1 h / Reflux View Scheme |
3-chloro-trans-2-[β-(dimethylamino)vinyl]-nitrobenzene
4-chloro-1H-indole
Conditions | Yield |
---|---|
With acetic acid; zinc In methanol; dichloromethane Heating; | 74% |
With hydrazine hydrate In tetrahydrofuran; methanol at 10 - 20℃; Reduction; cyclization; | 243.3 g |
In benzene |
2,β-Dinitro-6-chlor-styrol
4-chloro-1H-indole
Conditions | Yield |
---|---|
With indium; acetic acid In benzene at 80℃; for 1h; Inert atmosphere; | 74% |
N-(3-chloro-2-(2-(trimethylsilyl)ethynyl)phenyl)-2-hydroxy-2-methylpropanamide
4-chloro-1H-indole
Conditions | Yield |
---|---|
With sodium hydroxide In N,N-dimethyl-formamide at 140℃; for 4h; Inert atmosphere; | 73% |
With sodium hydroxide In N,N-dimethyl-formamide at 140℃; for 4h; Inert atmosphere; | 73% |
4-chloroindoline
4-chloro-1H-indole
Conditions | Yield |
---|---|
With oxygen; sodium t-butanolate In dimethyl sulfoxide at 60℃; under 760.051 Torr; for 4h; | 63% |
With monoamine oxidase D11 In aq. phosphate buffer; dimethyl sulfoxide at 37℃; for 168h; pH=7.8; Enzymatic reaction; | 44% |
methyl 4-chloro-3-indolecarboxylate
4-chloro-1H-indole
Conditions | Yield |
---|---|
With sodium hydroxide In methanol for 1.5h; Heating; | 61.7% |
6-chloro-2-nitrotoluene
N,N-dimethyl-formamide dimethyl acetal
4-chloro-1H-indole
Conditions | Yield |
---|---|
Stage #1: 6-chloro-2-nitrotoluene; N,N-dimethyl-formamide dimethyl acetal With pyrrolidine In 1,4-dioxane at 102℃; for 9h; Leimgruber-Batcho Indole Synthesis; Reflux; Inert atmosphere; Stage #2: With hydrazine hydrate In 1,4-dioxane at 45℃; for 1h; Leimgruber-Batcho Indole Synthesis; | 55% |
Stage #1: 6-chloro-2-nitrotoluene; N,N-dimethyl-formamide dimethyl acetal With pyrrolidine In N,N-dimethyl-formamide at 110℃; for 8h; Leimgruber-Batcho indole synthesis; Inert atmosphere; Stage #2: With iron(III) chloride hexahydrate; pyrographite; hydrazine hydrate In ethanol at 75℃; for 5h; Leimgruber-Batcho indole synthesis; |
4-Chloro-1-methoxy-1,3-dihydro-indol-2-one
4-chloro-1H-indole
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether for 3h; Heating; | 40% |
3-Chloronitrobenzene
vinyl magnesium bromide
A
6-chloroindole
B
4-chloro-1H-indole
C
3-chloro-aniline
Conditions | Yield |
---|---|
In tetrahydrofuran at -40℃; Yield given; | A n/a B n/a C 32% |
In tetrahydrofuran at -40℃; Yields of byproduct given; | A n/a B n/a C 32% |
1-[(E)-2-(2-chloro-6-nitrophenyl)vinyl]pyrrolidine
4-chloro-1H-indole
Conditions | Yield |
---|---|
With iron(III) chloride hexahydrate; pyrographite; hydrazine hydrate In ethanol at 75℃; for 5h; | 32% |
4-chloro-1H-indole-2-carboxylic acid
4-chloro-1H-indole
Conditions | Yield |
---|---|
With quinoline; copper(l) chloride Erhitzen auf Siedetemp.; | |
With quinoline; copper oxide-chromium oxide at 215℃; | |
at 255℃; |
4-chloro-1H-indole
Conditions | Yield |
---|---|
With titanium(III) chloride; ammonium acetate In acetone Yield given; |
6-chloro-2-nitrotoluene
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 89 percent / CuI; DMF / 0.33 h / 180 °C / 6000.6 - 7500.75 Torr / microwave irradiation 2: 74 percent / Zn; AcOH / methanol; CH2Cl2 / Heating View Scheme | |
Multi-step reaction with 2 steps 1: dimethylformamide / 80 h / 110 °C 2: 243.3 g / aq. hydrazine hydrate / tetrahydrofuran; methanol / 10 - 20 °C View Scheme | |
Multi-step reaction with 3 steps 1: DMSO, TritonB / methanol 2: H2 / 5percent Pd-C / ethyl acetate 3: 80 percent / RuCl2(PPh3)3 / toluene / Heating View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) Triton B, 2.) Zn, CaCl2 / 1.) Me2SO, 95 deg C, 1 h, 2.) H2O, reflux 2: 92 percent / RuCl2(PPh3)3 / toluene / 6 h / Heating View Scheme |
4-nitro-1H-indoIe
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: sodium hydride / N,N-dimethyl-formamide / 4 h 2: titanium(III) chloride / methanol; water / 0.12 h / Ambient temperature 3: hydrogenchloride; copper(l) chloride; sodium nitrite / 1.) water, 5 deg C, 20 min, 2.) water, room temp., 30 min; 97 deg C, 5 min 4: sodium hydroxide / methanol / 0.25 h / Heating View Scheme |
1-hydroxy-4-nitroindole
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: triethylamine / methanol / 16 h / Ambient temperature 2: sodium hydride / N,N-dimethyl-formamide / 4 h 3: titanium(III) chloride / methanol; water / 0.12 h / Ambient temperature 4: hydrogenchloride; copper(l) chloride; sodium nitrite / 1.) water, 5 deg C, 20 min, 2.) water, room temp., 30 min; 97 deg C, 5 min 5: sodium hydroxide / methanol / 0.25 h / Heating View Scheme | |
Multi-step reaction with 5 steps 1: triethylamine / methanol / 43 h / Ambient temperature 2: sodium hydride / N,N-dimethyl-formamide / 4 h 3: titanium(III) chloride / methanol; water / 0.12 h / Ambient temperature 4: hydrogenchloride; copper(l) chloride; sodium nitrite / 1.) water, 5 deg C, 20 min, 2.) water, room temp., 30 min; 97 deg C, 5 min 5: sodium hydroxide / methanol / 0.25 h / Heating View Scheme | |
Multi-step reaction with 5 steps 1: ethyl bromoacetate; triethylamine / methanol / 92.5 h / Ambient temperature 2: sodium hydride / N,N-dimethyl-formamide / 4 h 3: titanium(III) chloride / methanol; water / 0.12 h / Ambient temperature 4: hydrogenchloride; copper(l) chloride; sodium nitrite / 1.) water, 5 deg C, 20 min, 2.) water, room temp., 30 min; 97 deg C, 5 min 5: sodium hydroxide / methanol / 0.25 h / Heating View Scheme | |
Multi-step reaction with 6 steps 1: triethylamine / methanol / 16 h / Ambient temperature 2: triethylamine / methanol / 16 h / Ambient temperature 3: sodium hydride / N,N-dimethyl-formamide / 4 h 4: titanium(III) chloride / methanol; water / 0.12 h / Ambient temperature 5: hydrogenchloride; copper(l) chloride; sodium nitrite / 1.) water, 5 deg C, 20 min, 2.) water, room temp., 30 min; 97 deg C, 5 min 6: sodium hydroxide / methanol / 0.25 h / Heating View Scheme |
4-amino-1-methoxycarbonylindole
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: hydrogenchloride; copper(l) chloride; sodium nitrite / 1.) water, 5 deg C, 20 min, 2.) water, room temp., 30 min; 97 deg C, 5 min 2: sodium hydroxide / methanol / 0.25 h / Heating View Scheme |
1-methoxycarbonyl-4-nitroindole
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: titanium(III) chloride / methanol; water / 0.12 h / Ambient temperature 2: hydrogenchloride; copper(l) chloride; sodium nitrite / 1.) water, 5 deg C, 20 min, 2.) water, room temp., 30 min; 97 deg C, 5 min 3: sodium hydroxide / methanol / 0.25 h / Heating View Scheme |
methyl 2-hydroxy-2-(4-nitroindol-1-yl)-acetate
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: sodium hydrogencarbonate / methanol; water / 0.08 h / Heating 2: sodium hydride / N,N-dimethyl-formamide / 4 h 3: titanium(III) chloride / methanol; water / 0.12 h / Ambient temperature 4: hydrogenchloride; copper(l) chloride; sodium nitrite / 1.) water, 5 deg C, 20 min, 2.) water, room temp., 30 min; 97 deg C, 5 min 5: sodium hydroxide / methanol / 0.25 h / Heating View Scheme |
methyl 2-(4-nitroindole-1-yl)oxyacetate
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: triethylamine / methanol / 16 h / Ambient temperature 2: sodium hydride / N,N-dimethyl-formamide / 4 h 3: titanium(III) chloride / methanol; water / 0.12 h / Ambient temperature 4: hydrogenchloride; copper(l) chloride; sodium nitrite / 1.) water, 5 deg C, 20 min, 2.) water, room temp., 30 min; 97 deg C, 5 min 5: sodium hydroxide / methanol / 0.25 h / Heating View Scheme |
3-methoxycarbonylindole
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) TTFA, 2.) CuCl2 / 1.) TFA, room temp., 2 h; 2.) DMF, 120 deg C, 1 h 2: 61.7 percent / 40percent NaOH / methanol / 1.5 h / Heating View Scheme |
2-(2-chlorophenyl)-N-methoxyacetamide
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 97 percent / tert-butyl hypochlorite / CH2Cl2 / 0.33 h / 0 °C 2: 71 percent / Ag2CO3, trifluoroacetic acid / 0.5 h / 0 °C 3: 40 percent / LiAlH4 / diethyl ether / 3 h / Heating View Scheme |
N-chloro-2-(2-chlorophenyl)-N-methoxyacetamide
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 71 percent / Ag2CO3, trifluoroacetic acid / 0.5 h / 0 °C 2: 40 percent / LiAlH4 / diethyl ether / 3 h / Heating View Scheme |
2-(2-chlorophenyl)acetyl chloride
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 94 percent / sodium carbonate / H2O; benzene / 5 h / Ambient temperature 2: 97 percent / tert-butyl hypochlorite / CH2Cl2 / 0.33 h / 0 °C 3: 71 percent / Ag2CO3, trifluoroacetic acid / 0.5 h / 0 °C 4: 40 percent / LiAlH4 / diethyl ether / 3 h / Heating View Scheme |
(2-chloro-6-nitro-phenyl)-pyruvic acid
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Fe(OH)2; aqueous NH3 2: copper (I)-chloride; quinoline / Erhitzen auf Siedetemp. View Scheme |
3-chloro-2-iodophenyl N,N-dimethyl O-carbamate
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: sodium hydroxide / ethanol / Reflux 2.1: sodium hydroxide / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere 2.2: 2 h / 20 °C / Inert atmosphere 3.1: sodium hydroxide / N,N-dimethyl-formamide / 2 h / 60 °C / Inert atmosphere 4.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; diethylamine / N,N-dimethyl-formamide / 5.5 h / 40 °C / Inert atmosphere 5.1: sodium hydroxide / N,N-dimethyl-formamide / 4 h / 140 °C / Inert atmosphere View Scheme |
N-(3-chloro-2-iodophenyl)-2-hydroxy-2-methylpropanamide
4-chloro-1H-indole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; diethylamine / N,N-dimethyl-formamide / 5.5 h / 40 °C / Inert atmosphere 2: sodium hydroxide / N,N-dimethyl-formamide / 4 h / 140 °C / Inert atmosphere View Scheme |
4-chloro-1H-indole
2-Bromoethyl methyl ether
5-chloro-1-(2-methoxyethyl)-1H-indole
Conditions | Yield |
---|---|
With sodium hydride; sodium iodide In N,N-dimethyl-formamide; mineral oil at 0℃; for 2.16667h; | 100% |
4-chloro-1H-indole
4-chloroindoline
Conditions | Yield |
---|---|
Stage #1: 4-chloro-1H-indole With sodium cyanoborohydride; acetic acid In N,N-dimethyl-formamide at 20℃; for 2h; Stage #2: With water; sodium hydroxide In N,N-dimethyl-formamide | 99% |
With sodium cyanoborohydride; acetic acid at 0 - 20℃; Inert atmosphere; | 89% |
With sodium cyanoborohydride; acetic acid for 3h; Ambient temperature; |
4-chloro-1H-indole
di-tert-butyl dicarbonate
tert-butyl 4-chloro-1H-indole-1-carboxylate
Conditions | Yield |
---|---|
With dmap In tetrahydrofuran at 20℃; | 99% |
With dmap In tetrahydrofuran at 20℃; for 16h; Inert atmosphere; Sealed tube; | 91% |
With dmap In dichloromethane at 20℃; for 0.75h; |
4-chloro-1H-indole
3-bromopropanal dimethyl acetal
Conditions | Yield |
---|---|
With potassium hydroxide In N,N-dimethyl-formamide at 50℃; for 5h; | 99% |
4-chloro-1H-indole
tert-butyl N-(phenyl(phenylsulfonyl)methyl)carbamate
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate In toluene at 20℃; for 48h; Friedel-Crafts Alkylation; Inert atmosphere; Schlenk technique; regioselective reaction; | 99% |
4-chloro-1H-indole
9-phenyl-fluoren-9-ol
Conditions | Yield |
---|---|
With scandium tris(trifluoromethanesulfonate) In dichloromethane at 60℃; for 4h; Sealed tube; | 98% |
Conditions | Yield |
---|---|
Stage #1: 4-chloro-1H-indole With sodium hydride In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: benzyl bromide In N,N-dimethyl-formamide at 20℃; for 20h; | 97% |
Stage #1: 4-chloro-1H-indole With potassium hydroxide In N,N-dimethyl-formamide at 0℃; for 0.5h; Stage #2: benzyl bromide In N,N-dimethyl-formamide at 0 - 20℃; | |
Stage #1: 4-chloro-1H-indole With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0 - 20℃; for 0.666667h; Inert atmosphere; Stage #2: benzyl bromide In N,N-dimethyl-formamide; mineral oil at 0 - 45℃; for 1h; Inert atmosphere; |
4-chloro-1H-indole
methyl oct-1-en-3-yl carbonate
Conditions | Yield |
---|---|
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; C39H51N2O3P In acetonitrile at 100℃; for 36h; enantioselective reaction; | 97% |
4-chloro-1H-indole
acetyl chloride
1-(4-chloro-1H-indol-1-yl)ethan-1-one
Conditions | Yield |
---|---|
With tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide In dichloromethane at 20℃; for 0.75h; | 96% |
With tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide In dichloromethane at 20℃; for 1h; Inert atmosphere; Sealed tube; | 64% |
4-chloro-1H-indole
carbon monoxide
butan-1-ol
butyl 4-chloro-1H-indole-1-carboxylate
Conditions | Yield |
---|---|
With bis-triphenylphosphine-palladium(II) chloride; oxygen; copper diacetate; dimethyl sulfoxide; triphenylphosphine In toluene at 100℃; under 760.051 Torr; for 36h; regioselective reaction; | 95% |
4-chloro-1H-indole
(allylsulfonyl)benzene
Conditions | Yield |
---|---|
With potassium tert-butylate In toluene at 22℃; for 0.166667h; Inert atmosphere; Sealed tube; regioselective reaction; | 95% |
4-chloro-1H-indole
N,N-Dimethylcarbamoyl chloride
Conditions | Yield |
---|---|
Stage #1: 4-chloro-1H-indole With sodium hydride In N,N-dimethyl-formamide at 75℃; for 3h; Inert atmosphere; Stage #2: N,N-Dimethylcarbamoyl chloride In N,N-dimethyl-formamide at 75℃; Inert atmosphere; | 94% |
Stage #1: 4-chloro-1H-indole With sodium hydride In N,N-dimethyl-formamide at 0 - 75℃; Inert atmosphere; Schlenk technique; Stage #2: N,N-Dimethylcarbamoyl chloride In N,N-dimethyl-formamide at 0 - 75℃; Inert atmosphere; Schlenk technique; | 94% |
With potassium hydroxide 1.) THF, RT, 15 min, 2.) THF, RT, 4 h; Multistep reaction; | |
With tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide In dichloromethane Inert atmosphere; Reflux; |
4-chloro-1H-indole
Conditions | Yield |
---|---|
With bismuth(III) chloride In dichloromethane at 20℃; for 6h; | 94% |
Conditions | Yield |
---|---|
Stage #1: 4-chloro-1H-indole With sodium hydride In tetrahydrofuran at 0℃; for 1h; Stage #2: methyl iodide In tetrahydrofuran at 20℃; for 5h; | 93% |
Stage #1: 4-chloro-1H-indole With sodium hydride In tetrahydrofuran for 0.25h; Stage #2: methyl iodide In tetrahydrofuran | |
Stage #1: 4-chloro-1H-indole With sodium hydride In tetrahydrofuran for 0.25h; Stage #2: methyl iodide In tetrahydrofuran |
Conditions | Yield |
---|---|
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; diphenyl hydrogen phosphate; (R)-DTBM-BINAP at 60℃; Inert atmosphere; Glovebox; enantioselective reaction; | 93% |
Conditions | Yield |
---|---|
With potassium phosphate; palladium diacetate; ruphos In tetrahydrofuran; toluene at 100℃; for 15h; Suzuki-Miyaura Coupling; Schlenk technique; Inert atmosphere; | 93% |
4-chloro-1H-indole
benzenesulfonyl chloride
4-chloro-1-phenylsulfonyl-1H-indole
Conditions | Yield |
---|---|
Stage #1: 4-chloro-1H-indole With sodium hydride In tetrahydrofuran at 20℃; for 1h; Stage #2: benzenesulfonyl chloride In tetrahydrofuran for 1h; | 92% |
Stage #1: 4-chloro-1H-indole With sodium hydride In tetrahydrofuran at 0℃; Stage #2: benzenesulfonyl chloride In tetrahydrofuran at 0 - 20℃; |
Conditions | Yield |
---|---|
With iodine In dichloromethane at 20℃; for 1h; | 92% |
pyrrolidine
4-chloro-1H-indole
3-Chlorobenzaldehyde
4-chloro-3-((3-chlorophenyl)(pyrrolidin-1-yl)methyl)-1H-indole
Conditions | Yield |
---|---|
In methanol at 30℃; for 72h; | 92% |
4-chloro-1H-indole
ethyl 2-(4-methoxyphenyl)-6-methyl-3,4-dihydro-2H-pyran-5-carboxylate
ethyl 2-acetyl-5-(4-chloro-1H-indol-3-yl)-5-(4-methoxyphenyl)pentanoate
Conditions | Yield |
---|---|
With manganese(II) chloride tetrahydrate In nitromethane at 80℃; for 23h; | 91% |
Conditions | Yield |
---|---|
Stage #1: 4-chloro-1H-indole With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.5h; Cooling with ice; Inert atmosphere; Stage #2: benzyl chloride In N,N-dimethyl-formamide; mineral oil at 0 - 20℃; for 15h; Inert atmosphere; | 91% |
4-chloro-1H-indole
cyclopropanemethylamine
N-(cyclopropylmethyl)-1H-indol-4-amine
Conditions | Yield |
---|---|
With dicyclohexyl-(2′,4′,6′-triisopropyl-3,6-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine; chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2’,4’,6’-triisopropyl-1,1’-biphenyl] [2-(2-aminoethyl)phenyl]palladium(II); lithium hexamethyldisilazane In tetrahydrofuran at 80℃; for 4h; Inert atmosphere; Sealed vial; | 90% |
9-hydroxyxanthene
4-chloro-1H-indole
4-chloro-3-(9H-xanthen-9-yl)-1H-indole
Conditions | Yield |
---|---|
With betaine dihydrogenphosphate In octanol at 50℃; | 90% |
at 20℃; Ionic liquid; | 85% |
With 1,3-dichloro-1,1,3,3-tetrabutylstannoxane In dichloromethane at 20℃; for 10h; | 85% |
4-chloro-1H-indole
benzoyl chloride
(4-chloro-1H-indol-1-yl)(phenyl)methanone
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 14h; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
With L-proline In ethanol at 20℃; for 72h; | 90% |
4-chloro-1H-indole
methyldiphenylsilane
Conditions | Yield |
---|---|
With dodecacarbonyl-triangulo-triruthenium In toluene at 120℃; for 16h; Schlenk technique; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
With oxygen In tetrahydrofuran at 25℃; under 750.075 Torr; for 10h; Irradiation; | 90% |
With copper(II) choride dihydrate; oxygen In ethanol at 20℃; for 24h; Irradiation; | 86% |
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