Conditions | Yield |
---|---|
With potassium hydroxide In ethanol for 1h; Ambient temperature; | 99% |
With potassium hydroxide In water at 0 - 20℃; for 60h; | 71% |
With potassium hydroxide In ethanol; water for 4h; Heating; |
monomethyl monopotassium malonate
methyl-propanedioic acid
Conditions | Yield |
---|---|
With concentrated hydrochloric acid In water | 96% |
With hydrogenchloride In hexane; dichloromethane | 84.8% |
1,3-di-tert-butyl 2-methylpropanedioate
methyl-propanedioic acid
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; dichloromethane at 20℃; for 3h; Solvent; | 84% |
Conditions | Yield |
---|---|
In water; toluene | 81% |
With sodium hydroxide In methanol at 20℃; | |
With water; sodium hydroxide In methanol at 80℃; for 1h; |
Conditions | Yield |
---|---|
With potassium hydroxide |
2-methylmalonyl dichloride
methyl-propanedioic acid
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
With nitric acid |
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
Kochen; |
Conditions | Yield |
---|---|
Erhitzen; |
methyl-malonyl bromide
methyl-propanedioic acid
Conditions | Yield |
---|---|
With water |
Conditions | Yield |
---|---|
at 225℃; folgendes Verseifen mit Wasser; | |
at 225℃; im Rohr; und folgende Hydrolyse; | |
at 225℃; folgendes Verseifen mit Wasser; |
potassium cyanide
Ethyl 2-bromopropionate
methyl-propanedioic acid
Conditions | Yield |
---|---|
With ethanol ueber mehreren Stufen; |
2-methyl-3-oxo-3-(phenylamino)propanoic acid
methyl-propanedioic acid
Conditions | Yield |
---|---|
With sodium hydroxide Heating; |
Conditions | Yield |
---|---|
1.) Al, AlCl3, methylcyclohexane, 3 atm, 90-95 deg C, 12h; 2.) methylcyclohexane, 75 atm, 80 deg C; Multistep reaction; |
Conditions | Yield |
---|---|
With sodium bromate; sulfuric acid; cerium (IV) sulfate In water at 25℃; Mechanism; |
ethyl 2-nitrophenyl methylmalonate
A
ethanol
B
methyl-propanedioic acid
C
2-hydroxynitrobenzene
Conditions | Yield |
---|---|
With pH = 8.00 In water at 23℃; under 750.06 Torr; Mechanism; Rate constant; pressure-dependence of rates of elimination; activation parameter for hydrolysis: ΔV(excit.); var. press.; |
3,3-Dihydroxy-2-methyl-acrylic acid
methyl-propanedioic acid
Conditions | Yield |
---|---|
With cis-nitrous acid; chloride In water at 25℃; Equilibrium constant; |
Conditions | Yield |
---|---|
With sodium; Petroleum ether at 110℃; unter Druck; |
Conditions | Yield |
---|---|
With sodium; Petroleum ether at 110℃; unter Druck; |
methyl-propanedioic acid
Conditions | Yield |
---|---|
With sodium hydroxide |
methyl-propanedioic acid
Conditions | Yield |
---|---|
Erhitzen; |
ethyl 3-bromo-2-(ethoxycarbonyl)propionate
acetic acid
methyl-propanedioic acid
4-cyano-2-methyl-3-oxo-valeric acid ethyl ester
A
methyl-propanedioic acid
B
propionic acid
Conditions | Yield |
---|---|
Hydrolysis; |
chloroethane
carbon dioxide
A
methyl-propanedioic acid
B
propionic acid
Conditions | Yield |
---|---|
at 110℃; under 11032.6 Torr; |
9-hydroxyxanthene
methyl-propanedioic acid
(±)-2-(9H-xanthen-9-yl)propanoic acid
Conditions | Yield |
---|---|
With pyrrolidine; isopropyl alcohol; potassium hydroxide In toluene for 24h; Reflux; | 99% |
With pyridine |
5-(4'-fluorophenyl)furan-2-carbaldehyde
methyl-propanedioic acid
Conditions | Yield |
---|---|
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux; | 96.7% |
methyl-propanedioic acid
Conditions | Yield |
---|---|
With sodium hydroxide; nitric acid; silver nitrate In methanol; water | 96.7% |
methyl-propanedioic acid
4-(4-methylphenyl)thiophene-2-carbaldehyde
Conditions | Yield |
---|---|
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux; | 96.1% |
piperidine
methyl-propanedioic acid
tert-butyl (+/-)-trans-2,2-dimethyl-3-{2-carboxy-(E)-1-propenyl}cyclopropanecarboxylate
Conditions | Yield |
---|---|
In pyridine; diethyl ether; hexane; ethyl acetate | 96% |
In pyridine; diethyl ether; hexane; ethyl acetate | 94.1% |
4-phenylthiophene-2-carbaldehyde
methyl-propanedioic acid
(E)-2-methyl-3-(4-phenylthiophen-2-yl)acrylic acid
Conditions | Yield |
---|---|
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux; | 95.5% |
methyl-propanedioic acid
3-methyl-2-methylthio-6-(tetra-O-acetyl-β-D-glucopyranosylamino)pyrimidin-4(3H)-one
3,4,7,8-tetrahydro-5-hydroxy-3,6-dimethyl-2-methylthio-4,7-dioxo-8-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)pyrido<2,3-d>pyrimidine
Conditions | Yield |
---|---|
With acetic anhydride at 100℃; for 1h; | 95% |
methyl-propanedioic acid
di-tert-butyl dicarbonate
1,3-di-tert-butyl 2-methylpropanedioate
Conditions | Yield |
---|---|
With dmap In diethyl ether; tert-butyl alcohol at 23℃; for 48h; Inert atmosphere; | 95% |
methyl-propanedioic acid
Conditions | Yield |
---|---|
With calcium hydroxide In water at 70℃; for 5h; | 95% |
methyl-propanedioic acid
allyl alcohol
2-methylmalonic acid diallyl ester
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In benzene Heating; | 92% |
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 3.08333h; |
methyl-propanedioic acid
5-(4-tolyl)-2-furaldehyde
Conditions | Yield |
---|---|
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux; | 92% |
methyl-propanedioic acid
Conditions | Yield |
---|---|
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux; | 91.3% |
1,2-dimethoxybenzene
methyl-propanedioic acid
5,6-dimethoxy-2-methyl-1H-indene-1,3(2H)-dione
Conditions | Yield |
---|---|
In dichloromethane at 22℃; for 18h; | 91% |
With Eaton’s reagent In dichloromethane at 22℃; for 18h; Inert atmosphere; | 66% |
1-(2-fluoro-4-iodophenyl)-3-(4-methoxybenzyl)-6-(methylamino)pyrimidine-2,4(1H,3H)-dione
methyl-propanedioic acid
1-(2-fluoro-4-iodophenyl)-5-hydroxy-3-(4-methoxybenzyl)-6,8-dimethylpyrido[2,3-d]pyrimidine-2,4,7(1H,3H,8H)-trione
Conditions | Yield |
---|---|
With acetic anhydride at 90 - 100℃; for 4h; | 90.7% |
methyl-propanedioic acid
Conditions | Yield |
---|---|
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux; | 90.6% |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 3.08333h; | 90% |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 3.08333h; | 90% |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 3.08333h; | 90% |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 3.08333h; | 90% |
methyl-propanedioic acid
Conditions | Yield |
---|---|
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux; | 89.4% |
methyl-propanedioic acid
2,4,6-Trichlorophenol
bis(2,4,6-trichlorophenyl) 2-methylmalonate
Conditions | Yield |
---|---|
With trichlorophosphate for 5h; Reflux; | 89.11% |
With trichlorophosphate Reflux; |
N,N'-dimesitylformamidine
methyl-propanedioic acid
1,3-dimesityl-5-methyl-6-oxo-6H-pyrimidinium-4-olate
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 3h; Inert atmosphere; | 89% |
With triethylamine; dicyclohexyl-carbodiimide In dichloromethane at 0℃; Schlenk technique; Inert atmosphere; | 89% |
Conditions | Yield |
---|---|
With sodium carbonate In methanol; water three parts sepd. by water interphases: aq. soln. of MeCH(CO2H)2 and Na2CO3 at the bottom, soln. of Zn nitrate in the middle region and soln. ofbipyridine in MeOH on the top; sysztem stored at room temp. for a few w k; crystals collected; washed with H2O/EtOH; air dried; elem. anal.; | 89% |
Conditions | Yield |
---|---|
With manganese triacetate In acetic acid at 100℃; for 0.05h; | 88% |
methyl-propanedioic acid
Conditions | Yield |
---|---|
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux; | 87.7% |
methyl-propanedioic acid
1,1'-(4-nitro-phenylmethanediyl)-bis-piperidine
(E)-2-methyl-3-(4-nitrophenyl)acrylic acid
Conditions | Yield |
---|---|
for 96h; Ambient temperature; | 87% |
Conditions | Yield |
---|---|
With sodium carbonate In methanol; water three parts sepd. by water interphases: aq. soln. of MeCH(CO2H)2 and Na2CO3 at the bottom, soln. of CoCl2*6H2O in the middle region and soln. ofbipyridine in MeOH on the top; system stored at room temp. for a few wk; crystals collected; washed with H2O/EtOH; air dried; elem. anal.; | 87% |
methyl-propanedioic acid
Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-(2-methoxy-6-oxo-1,6-dihydro-pyrimidin-4-ylamino)-tetrahydro-pyran-3-yl ester
Conditions | Yield |
---|---|
With acetic anhydride at 100℃; for 1h; | 86% |
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