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inquiry2H-1,4-Benzoxazin-3(4H)-one Application:2H-1,4-Benzoxazin-3(4H)-one
(2-chloro-phenoxy)-acetic acid amide
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With chloro(2-dicyclohexylphosphino-2’,4’,6’-triisopropyl-1,1‘-biphenyl)[2-(2’-amino-1,1‘-biphenyl’)]palladium(II); caesium carbonate In 1,4-dioxane at 110℃; for 2h; Schlenk technique; Inert atmosphere; chemoselective reaction; | 99% |
Conditions | Yield |
---|---|
With copper acetylacetonate; sodium hydroxide; N,N`-dimethylethylenediamine In dichloromethane; N,N-dimethyl-formamide at 60℃; for 5h; Reagent/catalyst; | 97.6% |
Conditions | Yield |
---|---|
With copper(l) iodide; 1,10-Phenanthroline; caesium carbonate In 1,4-dioxane at 90℃; for 24h; Inert atmosphere; | 95% |
methanol
ethyl (2-hydroxyphenyl)carbamate
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With silica gel; potassium nitrate for 0.333333h; Reagent/catalyst; Concentration; Microwave irradiation; | 93.6% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In water for 4h; Reflux; | 93% |
With potassium carbonate In acetonitrile for 20h; Reflux; | 92.7% |
With sodium hydrogencarbonate; N-benzyl-N,N,N-triethylammonium chloride In chloroform 1.) 1 h, 0-5 deg C, 2.) 5 h, 55 deg C; | 89% |
2-(2-nitrophenoxy)acetonitrile
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With iron; acetic acid for 2.5h; Inert atmosphere; Reflux; | 93% |
With samarium; titanium tetrachloride In tetrahydrofuran at 20℃; for 0.166667h; reductive cyclization; | 70% |
With iron; acetic acid for 2h; Reflux; |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In water at 0℃; Reflux; | 93% |
ethyl o-nitrophenoxyacetate
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With iron; acetic acid at 0℃; for 7h; Inert atmosphere; Reflux; | 91% |
With iron In acetic acid at 0℃; for 7h; Inert atmosphere; Reflux; | 91% |
With iron In acetic acid at 0 - 20℃; for 2h; Reflux; | 74% |
N-(2-hydroxyphenyl)-2-chloroacetamide
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide for 10h; Reflux; | 88% |
With potassium carbonate In ethyl acetate at 20℃; for 10h; | 84% |
With alkali | |
With potassium carbonate In tetrahydrofuran for 2h; Reflux; Inert atmosphere; | 64.8 g |
With potassium tert-butylate In dichloromethane; isopropyl alcohol at 0 - 20℃; for 1h; |
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-octyl-3-methylimidazolium tetrafluoroborate at 20℃; for 1h; chemoselective reaction; | 86% |
Stage #1: ethyl bromoacetate; 2-amino-phenol With potassium fluoride In N,N-dimethyl-formamide at 60℃; Stage #2: With hydrogen; palladium on activated charcoal In ethanol at 60℃; under 7600 Torr; | 64% |
2-(2-nitrophenoxy)-acetic acid methyl ester
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With samarium; titanium tetrachloride In tetrahydrofuran at 20℃; for 0.166667h; reductive cyclization; | 75% |
With iron In acetic acid at 80℃; for 1h; |
6-bromo-3,4-dihydro-2H-1,4-benzoxazin-3-one
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; cesium acetate; isopropyl alcohol at 100℃; Schlenk technique; Inert atmosphere; | 72% |
With [RhCl2(p-cymene)]2; cesium acetate In isopropyl alcohol at 20 - 100℃; for 24h; Inert atmosphere; | 72% |
Conditions | Yield |
---|---|
With potassium carbonate In ethanol for 3h; Heating; | 70% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With polyphophoric acid at 65℃; for 2h; Reagent/catalyst; Temperature; | 56% |
2-Bromoacetyl bromide
2-amino-phenol
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
Stage #1: 2-amino-phenol With potassium carbonate In dichloromethane at 0℃; for 0.5h; Stage #2: 2-Bromoacetyl bromide In dichloromethane at 20℃; for 4h; | 55% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With polyphophoric acid at 60℃; for 2h; Reagent/catalyst; Temperature; | 52% |
(E)-3-benzylidene-4-tosyl-3,4-dihydro-2H-1,4-benzoxazine
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With naphthalene; sodium In tetrahydrofuran at -65℃; for 0.333333h; stereoselective reaction; | 50% |
6-chloromethyl-4-methyl-3-oxo-2,3-dihydro-4H-1,4-benzoxazine
N-methylbenzylamine hydrochloride
chloroacetyl chloride
2-amino-phenol
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; potassium carbonate In diethyl ether; hexane; chloroform | 32% |
6-chloro-4-hydroxy-(2H)-1,4-benzoxazin-3(4H)-one
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal | 30% |
7-chloro-4-hydroxy-2H-1,4-benzoxazin-3(4H)-one
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal | 30% |
2-phenoxyacetohydroxamic acid
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With iron(III) chloride In nitromethane at 60℃; for 2h; Reagent/catalyst; Temperature; | 30% |
Multi-step reaction with 2 steps 1: triethylamine / chloroform / 2 h / 0 - 20 °C 2: polyphophoric acid / 2 h / 60 °C View Scheme | |
Multi-step reaction with 2 steps 1: dmap / 3 h / 20 °C 2: polyphophoric acid / 2 h / 65 °C View Scheme |
N-(2-hydroxyphenyl)-2-chloroacetamide
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With sodium hydroxide; iron(II) sulfate | |
With iron; acetic acid | |
With ethanol; platinum Hydrogenation; |
2-chloro-N-(2-methoxyphenyl)acetamide
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With aluminium trichloride at 180℃; folgendes Behandeln mit wss. NaOH; |
Conditions | Yield |
---|---|
With hydrogenchloride |
2-azidocarbonylmethoxy-benzoyl azide
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With hydrogenchloride |
Conditions | Yield |
---|---|
With sodium; toluene anschliessend Erwaermen mit Chloressigsaeure-aethylester; | |
Multi-step reaction with 2 steps 1: Na2CO3 / CHCl3 / 3 h / Ambient temperature 2: K2CO3 / dimethylformamide / 3 h / 80 °C View Scheme | |
Multi-step reaction with 2 steps 1: benzene 2: alkali View Scheme |
6β-[2-(2-nitro-phenoxy)-acetylamino]-penicillanic acid
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With hydrogen; palladium In water |
2H-1,4-benzoxazin-3(4H)-thione
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With hydrogenchloride |
4-hydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
(i) AcCl, NaHCO3, CH2Cl2, (ii) PhOH; Multistep reaction; |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
acetic anhydride
4-acetoxy-(2H)-1,4-benzoxazin-3(4H)-one
Conditions | Yield |
---|---|
With pyridine for 12h; | 100% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
di-tert-butyl dicarbonate
tert-butyl 3-oxo-3,4-dihydro-2H-1,4-benzoxazine-4-carboxylate
Conditions | Yield |
---|---|
With dmap In acetonitrile at 20℃; for 48h; | 99% |
With dmap In tetrahydrofuran Ambient temperature; | 96% |
With dmap In tetrahydrofuran at 20℃; Acylation; | 96% |
With dmap In tetrahydrofuran at 20℃; for 3h; Acylation; | 96% |
With dmap In acetonitrile for 4h; |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
2-chloropropionyl chloride
6-(2-chloropropanoyl)-2H-1,4-benzoxazin-3(4H)-one
Conditions | Yield |
---|---|
With aluminum (III) chloride In 1,2-dichloro-ethane at 20℃; for 12h; | 99% |
3-chloromethyl-5-methylisoxazole
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide for 18h; Heating; | 99% |
Conditions | Yield |
---|---|
With [RuCl2(N-heterocyclic carbene)(bis[2-(diphenylphosphino)ethyl]amine)]; hydrogen; caesium carbonate In toluene; butan-1-ol at 120℃; under 22502.3 Torr; for 6h; Schlenk technique; Autoclave; | 98% |
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; for 2h; Inert atmosphere; | 92% |
Stage #1: 3,4-dihydro-3-oxo-2H-1,4-benzoxazine With lithium aluminium tetrahydride In tetrahydrofuran Heating / reflux; Stage #2: With sodium hydroxide; water In tetrahydrofuran | 79% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
ethyl bromoacetate
ethyl 2-(3-oxo-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)acetate
Conditions | Yield |
---|---|
Stage #1: 3,4-dihydro-3-oxo-2H-1,4-benzoxazine With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.25h; Stage #2: ethyl bromoacetate In N,N-dimethyl-formamide at 90℃; | 98% |
With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 3h; | 85% |
With potassium carbonate In methanol for 4h; Heating; | 77.4% |
With sodium hydride In N,N-dimethyl-formamide Ambient temperature; | 30% |
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 12h; |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
phenyl chloroformate
phenyl 2,3-dihydro-4H-1,4-benzoxazin-3-one-4-carboxylate
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran at -78℃; | 98% |
Stage #1: 3,4-dihydro-3-oxo-2H-1,4-benzoxazine With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h; Stage #2: phenyl chloroformate In tetrahydrofuran; hexane at 20℃; for 2h; |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
1,3-chlorobromopropane
4-(3-chloropropyl)-2H-1,4-benzoxazin-3(4H)-one
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 60h; | 97% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Ethyl 3-bromopropionate
ethyl 3-(3-oxo-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)propanoate
Conditions | Yield |
---|---|
Stage #1: 3,4-dihydro-3-oxo-2H-1,4-benzoxazine With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.25h; Stage #2: Ethyl 3-bromopropionate In N,N-dimethyl-formamide at 90℃; | 95% |
With potassium carbonate In N,N-dimethyl-formamide for 18h; Heating; | 91% |
With sodium hydride In N,N-dimethyl-formamide at 20℃; for 3h; | 45% |
Conditions | Yield |
---|---|
With acetic anhydride; triethylamine for 7h; Heating; | 94% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
4-methyl-4H-benzo[1,4]oxazin-3-one
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate In acetonitrile at 60℃; | 94% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
Bromoacetaldehyde diethyl acetal
4-(2,2-diethoxyethyl)-1,4-benzoxazin-3-one
Conditions | Yield |
---|---|
Stage #1: 3,4-dihydro-3-oxo-2H-1,4-benzoxazine With potassium tert-butylate In N,N-dimethyl acetamide at 20℃; for 0.0833333h; Stage #2: Bromoacetaldehyde diethyl acetal With tetra-(n-butyl)ammonium iodide In N,N-dimethyl acetamide at 80℃; for 2h; | 93.7% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
isonicotinoyl chloride hydrochloride
6-(1-pyridin-4-ylmethanoyl)-4H-benzo[1,4]oxazine-3-one hydrochloride
Conditions | Yield |
---|---|
With aluminum (III) chloride In N,N-dimethyl-formamide at 85℃; Friedel-Crafts Acylation; Inert atmosphere; | 93% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
propargyl bromide
4-(prop-2-yn-1-yl)-2H-benzo[b][1,4]oxazin-3(4H)-one
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 5h; Heating; | 92% |
With tetra-(n-butyl)ammonium iodide; potassium carbonate In N,N-dimethyl-formamide at 20℃; for 3h; Cooling with ice; | 92% |
With potassium carbonate In acetone; toluene Reflux; | 75% |
With potassium tert-butylate 1.) DMF, RT, 10 min, 2.) RT, 30 min; Yield given. Multistep reaction; | |
With potassium carbonate In acetone Inert atmosphere; Reflux; |
1,4-dibromo-butane
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
4-(4-Bromobutan-1-yl)-3,4-dihydro-2H-1,4-benzoxazin-3(4H)-one
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In acetonitrile at 100℃; | 92% |
Stage #1: 3,4-dihydro-3-oxo-2H-1,4-benzoxazine With sodium hydride In N,N-dimethyl-formamide; mineral oil at 30℃; for 1h; Cooling with ice; Stage #2: 1,4-dibromo-butane In N,N-dimethyl-formamide; mineral oil at 30℃; | 86% |
With aluminum oxide; potassium fluoride; potassium iodide In acetonitrile for 5h; Substitution; alkylation; Heating; |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
chloroacetyl chloride
6-(chloroacetyl)-2H-1,4-benzoxazin-3(4H)-one
Conditions | Yield |
---|---|
With aluminum (III) chloride In dichloromethane for 5.16h; Cooling with ice; Reflux; | 91% |
With aluminium trichloride In dichloromethane at 20℃; for 12h; Friedel-Crafts reaction; | 87.7% |
With aluminium trichloride In dichloromethane | 86% |
With aluminium trichloride | |
With aluminium trichloride In dichloromethane |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
2H-1,4-benzoxazin-3(4H)-thione
Conditions | Yield |
---|---|
With Lawessons reagent In tetrahydrofuran for 24h; Ambient temperature; | 91% |
With tetraphosphorus decasulfide; triethylamine In acetonitrile | 90% |
With tetraphosphorus decasulfide; N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate In 1,2-dichloro-ethane Heating; | 90% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
4-(2-bromoethyloxy)benzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 10h; | 91% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
4-(2-bromoethyloxy)benzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In water; ethyl acetate; N,N-dimethyl-formamide | 91% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
methyl iodide
4-methyl-4H-benzo[1,4]oxazin-3-one
Conditions | Yield |
---|---|
With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride; silica gel In acetonitrile for 0.133333h; Irradiation; | 90% |
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 2h; | 78.12% |
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 2h; | 78.12% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 60℃; for 36h; Reflux; | 90% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
2-Bromopropionyl chloride
6-(2-bromopropanoyl)-2H-1,4-benzoxazin-3(4H)-one
Conditions | Yield |
---|---|
With aluminum (III) chloride In 1,2-dichloro-ethane at 20℃; for 12h; | 89% |
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