sodium 1,4-diethoxy-1,4-dioxobut-2-en-2-olate
diethyl oxaloacetate
Conditions | Yield |
---|---|
With hydrogenchloride In diethyl ether; water | 83% |
Conditions | Yield |
---|---|
Stage #1: oxalic acid diethyl ester With sodium ethanolate In benzene at 0℃; Inert atmosphere; Stage #2: ethyl acetate In benzene at 0 - 20℃; for 14.5h; Inert atmosphere; | 74% |
With diethyl ether; sodium ethanolate Behandeln in Wasser mit verduennter Schwefelsaeure in Gegenwart von Aether; | |
With diethyl ether; sodium Behandeln in Wasser mit verduennter Schwefelsaeure in Gegenwart von Aether; |
Conditions | Yield |
---|---|
With water; platinum(II) chloride In methanol at 60℃; | 42% |
Conditions | Yield |
---|---|
With chloroform at 65℃; Behandeln des Reaktionsprodukts mit Aethanol.; |
Acetoxymaleinsaeureanhydrid
ethanol
A
ethyl acetate
B
diethyl oxaloacetate
Conditions | Yield |
---|---|
bei der Ozonspaltung; |
diethyl ether
sodium ethanolate
ethyl acetate
oxalic acid diethyl ester
diethyl oxaloacetate
ethanol
sodium ethanolate
ethyl acetate
oxalic acid diethyl ester
diethyl oxaloacetate
Ketene
chloroform
Ethyl oxalyl chloride
A
4,6-dioxo-5,6-dihydro-4H-pyran-2-carboxylic acid ethyl ester
B
oxalic acid diethyl ester
C
diethyl oxaloacetate
Conditions | Yield |
---|---|
anschliessenden Erwaermen mit Aethanol; |
Conditions | Yield |
---|---|
With sulfur dioxide at 65℃; Behandeln des Reaktionsprodukts mit Aethanol.; |
sodium ethanolate
oxalic acid diethyl ester
3-ethoxycarbonyl-3-penten-2-one
A
hydroxy-terephthalic acid diethyl ester
B
diethyl oxaloacetate
oxalic acid diethyl ester
3-ethoxycarbonyl-3-penten-2-one
A
hydroxy-terephthalic acid diethyl ester
B
diethyl oxaloacetate
Conditions | Yield |
---|---|
With ethanol; sodium ethanolate |
Dichlormethylenbrenztraubensaeureaethylester; Dichlorvinylglyoxylsaeureaethylester
sodium ethanolate
diethyl oxaloacetate
Conditions | Yield |
---|---|
In ethanol |
2-[(E)-1-Methyl-2-phenyl-ethylimino]-succinic acid diethyl ester
A
dexamfetamine
B
l-amphetamine
C
diethyl oxaloacetate
Conditions | Yield |
---|---|
With sulfuric acid In water for 2h; Ambient temperature; Yield given; |
2-[(E)-1-Phenyl-ethylimino]-succinic acid diethyl ester
A
(S)-1-phenyl-ethylamine
B
(R)-1-phenyl-ethyl-amine
C
diethyl oxaloacetate
Conditions | Yield |
---|---|
With sulfuric acid In water for 2h; Ambient temperature; Yield given; |
diethyl oxaloacetate
Conditions | Yield |
---|---|
Ozonolyse; |
Conditions | Yield |
---|---|
anschliessenden Behandeln mit Aethanol; |
diethyl ether
ethyl acetate
oxalic acid diethyl ester
diethyl oxaloacetate
ethanol
sodium ethanolate
ethyl acetate
oxalic acid diethyl ester
A
diethyl oxaloacetate
diethyl ether
ethyl acetate
oxalic acid diethyl ester
A
diethyl oxaloacetate
Ketene
oxalyl dichloride
A
3,4-dioxo-hexanedicarboxylic acid diethyl ester
B
diethyl oxaloacetate
Conditions | Yield |
---|---|
Behandeln des Reaktionsprodukts mit Aethanol; |
ethanol
imino-succinic acid diethyl ester
copper diacetate
acetic acid
A
ammonia
B
diethyl oxaloacetate
acetoxy-hydroxy-fumaric acid diethyl ester
A
oxalic acid
B
diethyl oxaloacetate
ozone
ethyl acetate
A
glyoxylic acid ethyl ester
B
diethyl oxaloacetate
Conditions | Yield |
---|---|
man erhaelt der Oxalessigester infolge des α-Cyan-aconitsaeure-triaethylester-Gehalts; |
L-aspartic acid diethyl ester
A
diethyl oxaloacetate
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: benzene / 72 h / Heating 2: H2 / 5percent palladium on charcoal / ethanol / 16 h / Ambient temperature 3: tert-butyl hypochlorite / diethyl ether / 0.5 h / 0 °C 4: sodium ethoxide / ethanol / 1 h / 40 °C 5: 5percent sulfuric acid / H2O / 2 h / Ambient temperature View Scheme | |
Multi-step reaction with 5 steps 1: benzene / 48 h / Heating 2: H2 / 5percent palladium on charcoal / ethanol / 16 h / Ambient temperature 3: tert-butyl hypochlorite / diethyl ether / 0.5 h / 0 °C 4: sodium ethoxide / ethanol / 1 h / 40 °C 5: 5percent sulfuric acid / H2O / 2 h / Ambient temperature View Scheme |
C16H22ClNO4
A
diethyl oxaloacetate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium ethoxide / ethanol / 1 h / 40 °C 2: 5percent sulfuric acid / H2O / 2 h / Ambient temperature View Scheme |
aminopyridin-2-ylacetic acid ethyl ester
diethyl oxaloacetate
Conditions | Yield |
---|---|
for 7h; Heating; | 8% |
Conditions | Yield |
---|---|
In ethanol for 16h; Heating; | 10% |
9-formyl-8-hydroxyjulolidine
diethyl oxaloacetate
Oxo-(10-oxo-2,3,5,6-tetrahydro-1H,4H,10H-11-oxa-3a-aza-benzo[de]anthracen-9-yl)-acetic acid ethyl ester
Conditions | Yield |
---|---|
With piperidine In acetonitrile for 120h; Heating; | 12% |
L-threonine methyl ester
diethyl oxaloacetate
diethyl 2-N-(2-hydroxy-1-methoxycarbonylpropylamino)but-2-enedioate
Conditions | Yield |
---|---|
With sodium sulfate In dichloromethane for 65h; Ambient temperature; | 13% |
diethyl oxaloacetate
Conditions | Yield |
---|---|
With acetic acid In benzene for 64h; Heating; | 16% |
5,5-dimethyl-6-hydrazino-4,5-dihydro-2H-pyridazin-3-one
diethyl oxaloacetate
Conditions | Yield |
---|---|
In ethanol at 20℃; for 120h; | 17% |
[2,4,5,6-2H4]3-chloroaniline
diethyl oxaloacetate
Conditions | Yield |
---|---|
In acetic acid at 45℃; | 17% |
Conditions | Yield |
---|---|
With acetic acid In benzene for 50h; Heating; | 19% |
chloroacetone
diethyl oxaloacetate
ethyl 3-hydroxy-6-methyl-2-oxo-1,2-dihydropyridine-4-carboxylate
Conditions | Yield |
---|---|
Stage #1: chloroacetone; diethyl oxaloacetate With ammonia In tetrahydrofuran for 0.666667h; Stage #2: With aluminum (III) chloride In tetrahydrofuran at 23℃; for 96h; | 19% |
Dimethylaminoguanidin*HBr
diethyl oxaloacetate
3-Dimethylamino-5-oxo-dihydro-1,2,4-triazin-6-yl-essigsaeureethylester
Conditions | Yield |
---|---|
With sodium acetate In ethanol for 12h; Heating; | 20% |
diethyl oxaloacetate
Conditions | Yield |
---|---|
With acetic acid In benzene for 40h; Heating; | 20% |
diethyl oxaloacetate
5-amino-1-methyl-2-phenylindole
Conditions | Yield |
---|---|
With acetic acid In benzene for 61h; Heating; | 21% |
6-Chloro-pyridin-3-ylamine
diethyl oxaloacetate
(6-chloro-pyridin-3-ylamino)-butenedioic acid diethyl ester
Conditions | Yield |
---|---|
at 90℃; for 7h; | 21% |
pyridine-2-carbaldehyde
diethyl oxaloacetate
diethyl 2,5-di(pyridin-2-yl)-1H-pyrrole-3,4-dicarboxylate
Conditions | Yield |
---|---|
With ammonium acetate In ethanol Reflux; | 22% |
diethyl oxaloacetate
Conditions | Yield |
---|---|
With acetic acid In benzene for 33h; Heating; | 23% |
4-Hydroxy-2-quinolone
diethyl oxaloacetate
2,5-Dioxo-5,6-dihydro-2H-pyrano<3,2-c>quinolinyl-4-carboxylic acid ethyl ester
Conditions | Yield |
---|---|
With ammonium acetate In nitrobenzene at 220℃; for 0.5h; | 25% |
diethyl oxaloacetate
Conditions | Yield |
---|---|
In toluene at 45℃; for 6h; | 26% |
p-toluidine
cyclohexanecarbaldehyde
diethyl oxaloacetate
ethyl 2-cyclohexyl-4-hydroxy-5-oxo-1-(4-methylphenyl)-2,5-dihydro-1H-pyrrole-3-carboxylate
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 26% |
2,3-dimethyl-5-amino-6-methoxyindole
diethyl oxaloacetate
Conditions | Yield |
---|---|
With acetic acid In benzene for 29h; Heating; | 27% |
2,3-dimethyl-4-aminoindole
diethyl oxaloacetate
Conditions | Yield |
---|---|
With acetic acid In benzene for 44h; Heating; | 27% |
4-nitrobenzaldehdye
aniline
diethyl oxaloacetate
ethyl 4‑hydroxy‑2‑(4‑nitrophenyl)‑5‑oxo‑1‑phenyl‑2,5‑dihydro‑1H‑pyrrole‑3‑carboxylate
Conditions | Yield |
---|---|
In methanol; ethanol for 24h; Ambient temperature; | 28% |
benzaldehyde
p-toluidine
diethyl oxaloacetate
ethyl 4-hydroxy-5-oxo-2-phenyl-1-(p-tolyl)-2,5-dihydro-1H-pyrrole-3-carboxylate
Conditions | Yield |
---|---|
In ethanol at 20℃; for 24h; | 28% |
benzaldehyde
4-nitro-aniline
diethyl oxaloacetate
ethyl 4-hydroxy-1-(4-nitrophenyl)-5-oxo-2-phenyl-2,5-dihydro-1H-pyrrole-3-carboxylate
Conditions | Yield |
---|---|
In methanol; ethanol for 240h; Ambient temperature; | 30% |
benzaldehyde
4-bromo-aniline
diethyl oxaloacetate
ethyl 1-(4-bromophenyl)-2,5-dihydro-4-hydroxy-5-oxo-2-phenyl-1H-pyrrole-3-carboxylate
Conditions | Yield |
---|---|
In ethanol at 20℃; for 24h; | 30% |
4-chlorobenzylidenemalonodinitrile
diethyl oxaloacetate
6-Amino-4-(4-chloro-phenyl)-5-cyano-4H-pyran-2,3-dicarboxylic acid diethyl ester
Conditions | Yield |
---|---|
With morpholine In ethanol for 0.5h; Ambient temperature; | 30% |
4-methoxy-benzaldehyde
aniline
diethyl oxaloacetate
ethyl 4‑hydroxy‑2‑(4‑methoxyphenyl)‑5‑oxo‑1‑phenyl‑2,5‑dihydro‑1H‑pyrrole‑3‑carboxylate
Conditions | Yield |
---|---|
In methanol; ethanol for 72h; Ambient temperature; | 33% |
2-methyl-4-nitro-3-isoxazolin-5(2H)-one
diethyl oxaloacetate
Conditions | Yield |
---|---|
Stage #1: diethyl oxaloacetate With sodium In ethanol Stage #2: 2-methyl-4-nitro-3-isoxazolin-5(2H)-one In pyridine at 0 - 20℃; for 5h; Stage #3: With ammonium chloride In ethanol at 80℃; for 10h; Further stages.; | 33% |
Conditions | Yield |
---|---|
Ambient temperature; | A 33.1% B 5.9% C 32.9% D 20.5% |
5-amino-2,3-dimethylindole
diethyl oxaloacetate
Conditions | Yield |
---|---|
With acetic acid In benzene for 30h; Heating; | 34% |
diethyl oxaloacetate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide boiling; | 35% |
In N,N-dimethyl-formamide boiling; | 35% |
The Diethyl oxalacetate with cas registry number of 108-56-5, has the systematic name of diethyl 2-oxobutanedioate. And its IUPAC name is the same one. Besides this, it is also named Butanedioic acid, oxo-, diethyl ester.
Physical properties about this chemical are: (1)ACD/LogP: 0.68; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.68; (4)ACD/LogD (pH 7.4): 0.59; (5)ACD/BCF (pH 5.5): 1.93; (6)ACD/BCF (pH 7.4): 1.56; (7)ACD/KOC (pH 5.5): 55.65; (8)ACD/KOC (pH 7.4): 44.95; (9)#H bond acceptors: 5; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 7; (12)Polar Surface Area: 69.67 Å2; (13)Index of Refraction: 1.431; (14)Molar Refractivity: 42.69 cm3; (15)Molar Volume: 164.6 cm3; (16)Polarizability: 16.92×10-24cm3; (17)Surface Tension: 36.5 dyne/cm; (18)Enthalpy of Vaporization: 49.16 kJ/mol; (19)Vapour Pressure: 0.0175 mmHg at 25°C.
You can still convert the following datas into molecular structure:
(1)SMILES: O=C(C(=O)OCC)CC(=O)OCC;
(2)InChI: InChI=1/C8H12O5/c1-3-12-7(10)5-6(9)8(11)13-4-2/h3-5H2,1-2H3;
(3)InChIKey: JDXYSCUOABNLIR-UHFFFAOYAC;
(4)Std. InChI: InChI=1S/C8H12O5/c1-3-12-7(10)5-6(9)8(11)13-4-2/h3-5H2,1-2H3;
(5)Std. InChIKey: JDXYSCUOABNLIR-UHFFFAOYSA-N
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