Product Name

  • Name

    Diethyl oxalacetate

  • EINECS 203-594-1
  • CAS No. 108-56-5
  • Article Data47
  • CAS DataBase
  • Density 1.143 g/cm3
  • Solubility Insoluble in water
  • Melting Point <25 °C
  • Formula C8H12O5
  • Boiling Point 254.223 °C at 760 mmHg
  • Molecular Weight 188.18
  • Flash Point 106.406 °C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 108-56-5 (Diethyl oxalacetate)
  • Hazard Symbols
  • Synonyms Butanedioicacid, oxo-, diethyl ester (9CI);Oxalacetic acid, diethyl ester (6CI,7CI,8CI);2-Oxobutanedioic acid diethyl ester;Diethyl 2-oxosuccinate;Diethyl oxobutanedioate;Diethyloxosuccinate;NSC 68476;Oxalacetic ester;
  • PSA 72.83000
  • LogP 0.55450

Synthetic route

sodium 1,4-diethoxy-1,4-dioxobut-2-en-2-olate
40876-98-0, 88330-76-1, 125898-38-6

sodium 1,4-diethoxy-1,4-dioxobut-2-en-2-olate

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
With hydrogenchloride In diethyl ether; water83%
ethyl acetate
141-78-6

ethyl acetate

oxalic acid diethyl ester
95-92-1

oxalic acid diethyl ester

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
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;
acetylenedicarboxylic acid diethyl ester
762-21-0

acetylenedicarboxylic acid diethyl ester

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
With water; platinum(II) chloride In methanol at 60℃;42%
Ketene
463-51-4

Ketene

oxalyl dichloride
79-37-8

oxalyl dichloride

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
With chloroform at 65℃; Behandeln des Reaktionsprodukts mit Aethanol.;
Acetoxymaleinsaeureanhydrid
19064-79-0

Acetoxymaleinsaeureanhydrid

ethanol
64-17-5

ethanol

A

ethyl acetate
141-78-6

ethyl acetate

B

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Acetoxymaleinsaeureanhydrid
19064-79-0

Acetoxymaleinsaeureanhydrid

ethanol
64-17-5

ethanol

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

diethylitaconate
2409-52-1

diethylitaconate

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
bei der Ozonspaltung;
diethyl ether
60-29-7

diethyl ether

sodium ethanolate
141-52-6

sodium ethanolate

ethyl acetate
141-78-6

ethyl acetate

oxalic acid diethyl ester
95-92-1

oxalic acid diethyl ester

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

ethanol
64-17-5

ethanol

sodium ethanolate
141-52-6

sodium ethanolate

ethyl acetate
141-78-6

ethyl acetate

oxalic acid diethyl ester
95-92-1

oxalic acid diethyl ester

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Ketene
463-51-4

Ketene

chloroform
67-66-3

chloroform

Ethyl oxalyl chloride
4755-77-5

Ethyl oxalyl chloride

A

4,6-dioxo-5,6-dihydro-4H-pyran-2-carboxylic acid ethyl ester
108153-39-5

4,6-dioxo-5,6-dihydro-4H-pyran-2-carboxylic acid ethyl ester

B

oxalic acid diethyl ester
95-92-1

oxalic acid diethyl ester

C

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
anschliessenden Erwaermen mit Aethanol;
Ketene
463-51-4

Ketene

Ethyl oxalyl chloride
4755-77-5

Ethyl oxalyl chloride

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
With sulfur dioxide at 65℃; Behandeln des Reaktionsprodukts mit Aethanol.;
sodium ethanolate
141-52-6

sodium ethanolate

oxalic acid diethyl ester
95-92-1

oxalic acid diethyl ester

3-ethoxycarbonyl-3-penten-2-one
15301-37-8, 67556-07-4, 67556-08-5

3-ethoxycarbonyl-3-penten-2-one

A

hydroxy-terephthalic acid diethyl ester
74744-72-2

hydroxy-terephthalic acid diethyl ester

B

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

oxalic acid diethyl ester
95-92-1

oxalic acid diethyl ester

3-ethoxycarbonyl-3-penten-2-one
15301-37-8, 67556-07-4, 67556-08-5

3-ethoxycarbonyl-3-penten-2-one

A

hydroxy-terephthalic acid diethyl ester
74744-72-2

hydroxy-terephthalic acid diethyl ester

B

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
With ethanol; sodium ethanolate
Dichlormethylenbrenztraubensaeureaethylester; Dichlorvinylglyoxylsaeureaethylester
16493-86-0

Dichlormethylenbrenztraubensaeureaethylester; Dichlorvinylglyoxylsaeureaethylester

sodium ethanolate
141-52-6

sodium ethanolate

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
In ethanol
2-[(E)-1-Methyl-2-phenyl-ethylimino]-succinic acid diethyl ester
87670-07-3

2-[(E)-1-Methyl-2-phenyl-ethylimino]-succinic acid diethyl ester

A

dexamfetamine
51-64-9

dexamfetamine

B

l-amphetamine
156-34-3

l-amphetamine

C

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
With sulfuric acid In water for 2h; Ambient temperature; Yield given;
2-[(E)-1-Phenyl-ethylimino]-succinic acid diethyl ester
87670-11-9

2-[(E)-1-Phenyl-ethylimino]-succinic acid diethyl ester

A

(S)-1-phenyl-ethylamine
2627-86-3

(S)-1-phenyl-ethylamine

B

(R)-1-phenyl-ethyl-amine
3886-69-9

(R)-1-phenyl-ethyl-amine

C

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
With sulfuric acid In water for 2h; Ambient temperature; Yield given;
itaconic acid ethyl ester

itaconic acid ethyl ester

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
Ozonolyse;
Ketene
463-51-4

Ketene

Ethyl oxalyl chloride
4755-77-5

Ethyl oxalyl chloride

liquid sulfur dioxide

liquid sulfur dioxide

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
anschliessenden Behandeln mit Aethanol;
diethyl ether
60-29-7

diethyl ether

ethyl acetate
141-78-6

ethyl acetate

oxalic acid diethyl ester
95-92-1

oxalic acid diethyl ester

sodium

sodium

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

ethanol
64-17-5

ethanol

sodium ethanolate
141-52-6

sodium ethanolate

ethyl acetate
141-78-6

ethyl acetate

oxalic acid diethyl ester
95-92-1

oxalic acid diethyl ester

A

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

B

oxalcitric acid lactonetriethyl ester

oxalcitric acid lactonetriethyl ester

C

α-pyrone-tricarboxylic acid-(4.5.6)-triethyl ester

α-pyrone-tricarboxylic acid-(4.5.6)-triethyl ester

diethyl ether
60-29-7

diethyl ether

ethyl acetate
141-78-6

ethyl acetate

oxalic acid diethyl ester
95-92-1

oxalic acid diethyl ester

sodium

sodium

A

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

B

oxalcitric acid lactonetriethyl ester

oxalcitric acid lactonetriethyl ester

C

α-pyrone-tricarboxylic acid-(4.5.6)-triethyl ester

α-pyrone-tricarboxylic acid-(4.5.6)-triethyl ester

Ketene
463-51-4

Ketene

oxalyl dichloride
79-37-8

oxalyl dichloride

liquid sulfur dioxide

liquid sulfur dioxide

A

3,4-dioxo-hexanedicarboxylic acid diethyl ester
3249-69-2

3,4-dioxo-hexanedicarboxylic acid diethyl ester

B

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

Conditions
ConditionsYield
Behandeln des Reaktionsprodukts mit Aethanol;
ethanol
64-17-5

ethanol

imino-succinic acid diethyl ester
52604-04-3

imino-succinic acid diethyl ester

copper diacetate
142-71-2

copper diacetate

acetic acid
64-19-7

acetic acid

A

ammonia
7664-41-7

ammonia

B

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

acetoxy-hydroxy-fumaric acid diethyl ester
114352-39-5

acetoxy-hydroxy-fumaric acid diethyl ester

air

air

aqueous solutions of pH > 11

aqueous solutions of pH > 11

A

oxalic acid
144-62-7

oxalic acid

B

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

hydrogenchloride
7647-01-0

hydrogenchloride

bis-(1,2-bis-ethoxycarbonyl-ethylidene)-guanidine

bis-(1,2-bis-ethoxycarbonyl-ethylidene)-guanidine

A

guanidine nitrate
113-00-8

guanidine nitrate

B

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

bis-(1,2-bis-ethoxycarbonyl-ethylidene)-guanidine

bis-(1,2-bis-ethoxycarbonyl-ethylidene)-guanidine

ammonia
7664-41-7

ammonia

A

guanidine nitrate
113-00-8

guanidine nitrate

B

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

3-cyano-propene-1,2,3-tricarboxylic acid triethyl ester

3-cyano-propene-1,2,3-tricarboxylic acid triethyl ester

ethyl acetate
141-78-6

ethyl acetate

A

glyoxylic acid ethyl ester
924-44-7

glyoxylic acid ethyl ester

B

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

C

oxalcyanoacetic acid diethyl ester

oxalcyanoacetic acid diethyl ester

Conditions
ConditionsYield
man erhaelt der Oxalessigester infolge des α-Cyan-aconitsaeure-triaethylester-Gehalts;
L-aspartic acid diethyl ester
13552-87-9

L-aspartic acid diethyl ester

A

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

B

bromoethoxycarbonylmethylene-4-nitro-phenylhydrazine

bromoethoxycarbonylmethylene-4-nitro-phenylhydrazine

Conditions
ConditionsYield
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

A

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

B

bromoethoxycarbonylmethylene-4-nitro-phenylhydrazine

bromoethoxycarbonylmethylene-4-nitro-phenylhydrazine

Conditions
ConditionsYield
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
55243-15-7

aminopyridin-2-ylacetic acid ethyl ester

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

ethyl 3-(1'-ethoxycarbonylimidazo<1,5-a>pyrid-3'-yl)-2-oxopropionate

ethyl 3-(1'-ethoxycarbonylimidazo<1,5-a>pyrid-3'-yl)-2-oxopropionate

Conditions
ConditionsYield
for 7h; Heating;8%
acetamidine
143-37-3

acetamidine

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

ethyl 2-methyl-6-oxo-1H-pyrimidine-4-carboxylate

ethyl 2-methyl-6-oxo-1H-pyrimidine-4-carboxylate

Conditions
ConditionsYield
In ethanol for 16h; Heating;10%
9-formyl-8-hydroxyjulolidine
63149-33-7

9-formyl-8-hydroxyjulolidine

diethyl oxaloacetate
108-56-5

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
118043-79-1

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
ConditionsYield
With piperidine In acetonitrile for 120h; Heating;12%
L-threonine methyl ester
3373-59-9

L-threonine methyl ester

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

diethyl 2-N-(2-hydroxy-1-methoxycarbonylpropylamino)but-2-enedioate
139370-60-8

diethyl 2-N-(2-hydroxy-1-methoxycarbonylpropylamino)but-2-enedioate

Conditions
ConditionsYield
With sodium sulfate In dichloromethane for 65h; Ambient temperature;13%
5-amino-1,2,3,6-tetramethylindole

5-amino-1,2,3,6-tetramethylindole

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

diethyl (5-amino-1,2,3,6-tetramethyl-1H-indolyl)fumarate

diethyl (5-amino-1,2,3,6-tetramethyl-1H-indolyl)fumarate

Conditions
ConditionsYield
With acetic acid In benzene for 64h; Heating;16%
5,5-dimethyl-6-hydrazino-4,5-dihydro-2H-pyridazin-3-one
100568-22-7

5,5-dimethyl-6-hydrazino-4,5-dihydro-2H-pyridazin-3-one

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

diethyl 2-[(1,4,5,6-tetrahydro-4,4-dimethyl-6-oxo-3-pyridazinyl)hydrazono]butanedioate

diethyl 2-[(1,4,5,6-tetrahydro-4,4-dimethyl-6-oxo-3-pyridazinyl)hydrazono]butanedioate

Conditions
ConditionsYield
In ethanol at 20℃; for 120h;17%
[2,4,5,6-2H4]3-chloroaniline
1027104-24-0

[2,4,5,6-2H4]3-chloroaniline

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

1,4-diethyl (2E)-2-[[3-chloro(2H4)phenyl]imino]butanedioate

1,4-diethyl (2E)-2-[[3-chloro(2H4)phenyl]imino]butanedioate

Conditions
ConditionsYield
In acetic acid at 45℃;17%
5-amino-2-methylindole
7570-49-2

5-amino-2-methylindole

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

diethyl (5-amino-2-methyl-1H-indolyl)fumarate

diethyl (5-amino-2-methyl-1H-indolyl)fumarate

Conditions
ConditionsYield
With acetic acid In benzene for 50h; Heating;19%
chloroacetone
78-95-5

chloroacetone

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

ethyl 3-hydroxy-6-methyl-2-oxo-1,2-dihydropyridine-4-carboxylate
267876-32-4

ethyl 3-hydroxy-6-methyl-2-oxo-1,2-dihydropyridine-4-carboxylate

Conditions
ConditionsYield
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
13750-16-8

Dimethylaminoguanidin*HBr

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

3-Dimethylamino-5-oxo-dihydro-1,2,4-triazin-6-yl-essigsaeureethylester
112080-99-6

3-Dimethylamino-5-oxo-dihydro-1,2,4-triazin-6-yl-essigsaeureethylester

Conditions
ConditionsYield
With sodium acetate In ethanol for 12h; Heating;20%
5-amino-1,6-dimethyl-2-phenylindole

5-amino-1,6-dimethyl-2-phenylindole

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

diethyl (5-amino-1,6-dimethyl-2-phenyl-1H-indolyl)fumarate

diethyl (5-amino-1,6-dimethyl-2-phenyl-1H-indolyl)fumarate

Conditions
ConditionsYield
With acetic acid In benzene for 40h; Heating;20%
diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

5-amino-1-methyl-2-phenylindole
748799-33-9

5-amino-1-methyl-2-phenylindole

diethyl (5-amino-1-methyl-2-phenyl-1H-indolyl)fumarate

diethyl (5-amino-1-methyl-2-phenyl-1H-indolyl)fumarate

Conditions
ConditionsYield
With acetic acid In benzene for 61h; Heating;21%
6-Chloro-pyridin-3-ylamine
5350-93-6

6-Chloro-pyridin-3-ylamine

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

(6-chloro-pyridin-3-ylamino)-butenedioic acid diethyl ester
53241-89-7

(6-chloro-pyridin-3-ylamino)-butenedioic acid diethyl ester

Conditions
ConditionsYield
at 90℃; for 7h;21%
pyridine-2-carbaldehyde
1121-60-4

pyridine-2-carbaldehyde

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

diethyl 2,5-di(pyridin-2-yl)-1H-pyrrole-3,4-dicarboxylate
109694-41-9

diethyl 2,5-di(pyridin-2-yl)-1H-pyrrole-3,4-dicarboxylate

Conditions
ConditionsYield
With ammonium acetate In ethanol Reflux;22%
6-methyl-2-phenyl-1H-indol-5-ylamine

6-methyl-2-phenyl-1H-indol-5-ylamine

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

2-(6-methyl-2-phenyl-1H-indol-5-ylamino)-but-2-enedioic acid diethyl ester

2-(6-methyl-2-phenyl-1H-indol-5-ylamino)-but-2-enedioic acid diethyl ester

Conditions
ConditionsYield
With acetic acid In benzene for 33h; Heating;23%
4-Hydroxy-2-quinolone
70254-43-2, 70254-44-3

4-Hydroxy-2-quinolone

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

2,5-Dioxo-5,6-dihydro-2H-pyrano<3,2-c>quinolinyl-4-carboxylic acid ethyl ester
94192-47-9

2,5-Dioxo-5,6-dihydro-2H-pyrano<3,2-c>quinolinyl-4-carboxylic acid ethyl ester

Conditions
ConditionsYield
With ammonium acetate In nitrobenzene at 220℃; for 0.5h;25%
3-chloro(2,4,6-2H3)aniline

3-chloro(2,4,6-2H3)aniline

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

1,4-diethyl (2E)-2-[[3-chloro(2,4,6-2H3)phenyl]imino]butanedioate

1,4-diethyl (2E)-2-[[3-chloro(2,4,6-2H3)phenyl]imino]butanedioate

Conditions
ConditionsYield
In toluene at 45℃; for 6h;26%
p-toluidine
106-49-0

p-toluidine

cyclohexanecarbaldehyde
2043-61-0

cyclohexanecarbaldehyde

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

ethyl 2-cyclohexyl-4-hydroxy-5-oxo-1-(4-methylphenyl)-2,5-dihydro-1H-pyrrole-3-carboxylate
512178-20-0

ethyl 2-cyclohexyl-4-hydroxy-5-oxo-1-(4-methylphenyl)-2,5-dihydro-1H-pyrrole-3-carboxylate

Conditions
ConditionsYield
In tetrahydrofuran at 20℃;26%
2,3-dimethyl-5-amino-6-methoxyindole
135855-58-2

2,3-dimethyl-5-amino-6-methoxyindole

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

diethyl (5-amino-6-methoxy-2,3-dimethyl-1H-indolyl)fumarate

diethyl (5-amino-6-methoxy-2,3-dimethyl-1H-indolyl)fumarate

Conditions
ConditionsYield
With acetic acid In benzene for 29h; Heating;27%
2,3-dimethyl-4-aminoindole
135855-64-0

2,3-dimethyl-4-aminoindole

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

[(2,3-dimethyl-1H-indol-4-yl)amino]fumaric acid diethyl ester

[(2,3-dimethyl-1H-indol-4-yl)amino]fumaric acid diethyl ester

Conditions
ConditionsYield
With acetic acid In benzene for 44h; Heating;27%
4-nitrobenzaldehdye
555-16-8

4-nitrobenzaldehdye

aniline
62-53-3

aniline

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

ethyl 4‑hydroxy‑2‑(4‑nitrophenyl)‑5‑oxo‑1‑phenyl‑2,5‑dihydro‑1H‑pyrrole‑3‑carboxylate
131189-27-0

ethyl 4‑hydroxy‑2‑(4‑nitrophenyl)‑5‑oxo‑1‑phenyl‑2,5‑dihydro‑1H‑pyrrole‑3‑carboxylate

Conditions
ConditionsYield
In methanol; ethanol for 24h; Ambient temperature;28%
benzaldehyde
100-52-7

benzaldehyde

p-toluidine
106-49-0

p-toluidine

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

ethyl 4-hydroxy-5-oxo-2-phenyl-1-(p-tolyl)-2,5-dihydro-1H-pyrrole-3-carboxylate
147298-51-9

ethyl 4-hydroxy-5-oxo-2-phenyl-1-(p-tolyl)-2,5-dihydro-1H-pyrrole-3-carboxylate

Conditions
ConditionsYield
In ethanol at 20℃; for 24h;28%
benzaldehyde
100-52-7

benzaldehyde

4-nitro-aniline
100-01-6

4-nitro-aniline

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

ethyl 4-hydroxy-1-(4-nitrophenyl)-5-oxo-2-phenyl-2,5-dihydro-1H-pyrrole-3-carboxylate
131189-28-1

ethyl 4-hydroxy-1-(4-nitrophenyl)-5-oxo-2-phenyl-2,5-dihydro-1H-pyrrole-3-carboxylate

Conditions
ConditionsYield
In methanol; ethanol for 240h; Ambient temperature;30%
benzaldehyde
100-52-7

benzaldehyde

4-bromo-aniline
106-40-1

4-bromo-aniline

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

ethyl 1-(4-bromophenyl)-2,5-dihydro-4-hydroxy-5-oxo-2-phenyl-1H-pyrrole-3-carboxylate
139325-41-0

ethyl 1-(4-bromophenyl)-2,5-dihydro-4-hydroxy-5-oxo-2-phenyl-1H-pyrrole-3-carboxylate

Conditions
ConditionsYield
In ethanol at 20℃; for 24h;30%
4-chlorobenzylidenemalonodinitrile
1867-38-5

4-chlorobenzylidenemalonodinitrile

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

6-Amino-4-(4-chloro-phenyl)-5-cyano-4H-pyran-2,3-dicarboxylic acid diethyl ester
77151-43-0

6-Amino-4-(4-chloro-phenyl)-5-cyano-4H-pyran-2,3-dicarboxylic acid diethyl ester

Conditions
ConditionsYield
With morpholine In ethanol for 0.5h; Ambient temperature;30%
4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

aniline
62-53-3

aniline

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

ethyl 4‑hydroxy‑2‑(4‑methoxyphenyl)‑5‑oxo‑1‑phenyl‑2,5‑dihydro‑1H‑pyrrole‑3‑carboxylate
131189-26-9

ethyl 4‑hydroxy‑2‑(4‑methoxyphenyl)‑5‑oxo‑1‑phenyl‑2,5‑dihydro‑1H‑pyrrole‑3‑carboxylate

Conditions
ConditionsYield
In methanol; ethanol for 72h; Ambient temperature;33%
2-methyl-4-nitro-3-isoxazolin-5(2H)-one
138842-45-2

2-methyl-4-nitro-3-isoxazolin-5(2H)-one

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

2,3-bis(ethoxycarbonyl)-1-methyl-4-nitropyrrole

2,3-bis(ethoxycarbonyl)-1-methyl-4-nitropyrrole

Conditions
ConditionsYield
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%
methyl-1 amino-3 pyrazole
1904-31-0

methyl-1 amino-3 pyrazole

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

A

4-ethoxycarbonyl-2-methyl-2H-pyrazolo<3,4-b>pyridin-6(7H)-one

4-ethoxycarbonyl-2-methyl-2H-pyrazolo<3,4-b>pyridin-6(7H)-one

B

3-amino-4-(1,2-bis-ethoxycarbonylvinyl)-1-methylpyrazole

3-amino-4-(1,2-bis-ethoxycarbonylvinyl)-1-methylpyrazole

C

3-(1,2-bis-ethoxycarbonylvinylamino)-1-methylpyrazole

3-(1,2-bis-ethoxycarbonylvinylamino)-1-methylpyrazole

D

ethyl α-(3-amino-1-methyl-4-pyrazolyl)-β-acrylate

ethyl α-(3-amino-1-methyl-4-pyrazolyl)-β-acrylate

Conditions
ConditionsYield
Ambient temperature;A 33.1%
B 5.9%
C 32.9%
D 20.5%
5-amino-2,3-dimethylindole
16712-58-6

5-amino-2,3-dimethylindole

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

diethyl (5-amino-2,3-dimethyl-1H-indolyl)fumarate

diethyl (5-amino-2,3-dimethyl-1H-indolyl)fumarate

Conditions
ConditionsYield
With acetic acid In benzene for 30h; Heating;34%
N,N,N-(ferrocenylmethyl)trimethylammonium iodide

N,N,N-(ferrocenylmethyl)trimethylammonium iodide

diethyl oxaloacetate
108-56-5

diethyl oxaloacetate

(C10H9FeCH2)2C(COOC2H5)COCOOC2H5

(C10H9FeCH2)2C(COOC2H5)COCOOC2H5

Conditions
ConditionsYield
In N,N-dimethyl-formamide boiling;35%
In N,N-dimethyl-formamide boiling;35%

Diethyl oxalacetate Specification

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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