sodium methylate
N,N-dimethyl-formamide
N,N-dimethyl-formamide dimethyl acetal
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-formamide With dimethyl sulfate at 20 - 70℃; for 4h; Stage #2: sodium methylate at 25℃; for 2h; Temperature; | 85.4% |
dimethyl amine
trimethyl orthoformate
N,N-dimethyl-formamide dimethyl acetal
Conditions | Yield |
---|---|
With acetyl chloride at 20℃; for 12h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With sulfuric acid In 1,4-dioxane; water at 0℃; for 6h; Inert atmosphere; | 80% |
(methoxymethylidene)dimethylammonium methyl sulfate
N,N-dimethyl-formamide dimethyl acetal
Conditions | Yield |
---|---|
With methanol; sodium methylate at 0 - 20℃; for 20h; Inert atmosphere; | 59% |
chloro-dimethoxy-methane
dimethyl amine
N,N-dimethyl-formamide dimethyl acetal
Conditions | Yield |
---|---|
at 140 - 150℃; for 2h; Green chemistry; | 86.8% |
N,N-dimethyl-formamide
dimethyl sulfate
N,N-dimethyl-formamide dimethyl acetal
Conditions | Yield |
---|---|
With nitrogen at 80℃; for 2h; | 100% |
With sodium 1.) 3 h, 60-80 degC: 2.) 0 degC, methanol; Yield given. Multistep reaction; | |
at 60℃; for 3h; |
sodium methylate
(methoxymethylidene)dimethylammonium methyl sulfate
N,N-dimethyl-formamide dimethyl acetal
Conditions | Yield |
---|---|
In Petroleum ether at 0℃; for 2h; |
1-(2-furyl)-1-ethanone
A
N,N-dimethyl-formamide dimethyl acetal
B
(2E)-3-(dimethylamino)-1-furan-2-ylprop-2-en-1-one
methyl-3-pyridylketone
A
(E)-3-(dimethylamino)-1-(pyridin-3-yl)prop-2-en-1-one
B
N,N-dimethyl-formamide dimethyl acetal
N,N-dimethyl-formamide
2-butyl-2-imidazolin-5-one
N,N-dimethyl-formamide dimethyl acetal
Conditions | Yield |
---|---|
With trichlorophosphate at 40℃; Condensation; |
sodium methylate
N,N,N',N'-Tetramethylformamidinium chloride
A
bis(dimethylamino)methoxymethane
B
tris(dimethylamino)methane
C
N,N-dimethyl-formamide dimethyl acetal
Conditions | Yield |
---|---|
In tetrahydrofuran at 21℃; Title compound not separated from byproducts.; |
chloroform
sodium methylate
A
N,N-dimethyl-formamide dimethyl acetal
B
trimethyl orthoformate
Conditions | Yield |
---|---|
With N,N-dimethyl-formamide In methanol | A 48 % Chromat. B 38 % Chromat. |
chloroform
sodium methylate
N,N-dimethyl-formamide
A
N,N-dimethyl-formamide dimethyl acetal
B
trimethyl orthoformate
Conditions | Yield |
---|---|
A 91 % Chromat. B 3 % Chromat. |
chloroform
sodium methylate
N,N-dimethyl-formamide
A
carbon monoxide
B
N,N-dimethyl-formamide dimethyl acetal
C
trimethyl orthoformate
Conditions | Yield |
---|---|
for 0.5h; Mechanism; methanol presence; |
5-methyl-1,3,4-thiadiazol-2-amine
N,N-dimethyl-formamide dimethyl acetal
2-(N,N-dimethylaminomethyleneamino)-5-methyl-1,3,4-thiadiazole
Conditions | Yield |
---|---|
In toluene for 2h; Heating; | 100% |
In ethanol Heating; |
N,N-dimethyl-formamide dimethyl acetal
ethyl isopropylidenecyanoacetate
1-carbethoxy-1-cyano-2-methyl-4-dimethylamino-1,4-butadiene
Conditions | Yield |
---|---|
In ethanol for 24h; Heating / reflux; | 100% |
In ethanol for 24h; Reflux; | 74% |
In ethanol |
2-aminopyridine
N,N-dimethyl-formamide dimethyl acetal
N,N-dimethyl-N'-pyridin-2-yl-formamidine
Conditions | Yield |
---|---|
at 150℃; for 0.116667h; Microwave; | 100% |
In methanol at 70℃; for 15h; | 81% |
for 6h; Reflux; | 71% |
2-aminopyrimidine
N,N-dimethyl-formamide dimethyl acetal
N,N-dimethyl-N'-pyrimidin-2-ylformamidine
Conditions | Yield |
---|---|
In toluene Heating; | 100% |
for 6h; Reflux; | 80% |
In toluene for 2h; Heating; |
6-chloro-pyridazin-3-ylamine
N,N-dimethyl-formamide dimethyl acetal
N'-(6-chloropyridazin-3-yl)-N,N-dimethylmethanimidamide
Conditions | Yield |
---|---|
at 105℃; for 2h; | 100% |
for 2h; Reflux; | 81% |
for 2h; Reflux; | 81% |
2-methyl-3-nitropyridine
N,N-dimethyl-formamide dimethyl acetal
2-(3-nitro-2-pyridinyl)-N,N-dimethyletheneamine
Conditions | Yield |
---|---|
100% | |
In N,N-dimethyl-formamide at 90℃; for 4h; Inert atmosphere; | 73% |
In N,N-dimethyl-formamide at 115℃; | |
In N,N-dimethyl-formamide at 120℃; for 17h; |
Conditions | Yield |
---|---|
With potassium tert-butylate for 0.0833333h; Heating; | 100% |
isobutylamine
N,N-dimethyl-formamide dimethyl acetal
N2-iso-butyl-N1,N1-dimethylformamidine
Conditions | Yield |
---|---|
at 60℃; | 100% |
ethyl acetoacetate
N,N-dimethyl-formamide dimethyl acetal
ethyl 2-[(dimethylamino)methylene]-3-oxobutanoate
Conditions | Yield |
---|---|
at 20℃; | 100% |
at 20℃; | 100% |
at 20℃; | 100% |
1,3-cylohexanedione
N,N-dimethyl-formamide dimethyl acetal
2-(dimethylaminomethylene)cyclohexane-1,3-dione
Conditions | Yield |
---|---|
for 1h; Heating; | 100% |
at 100℃; for 1h; | 100% |
at 95℃; for 1h; | 100% |
ethyl 3-oxo-3-phenylpropionate
N,N-dimethyl-formamide dimethyl acetal
ethyl-3-(dimethylamino)-2-(phenylcarbonyl)prop-2-enoate
Conditions | Yield |
---|---|
at 110℃; for 0.666667h; Microwave irradiation; | 100% |
for 1h; Heating; | 94% |
In toluene at 60℃; for 24h; | 92% |
cyclohexylamine
N,N-dimethyl-formamide dimethyl acetal
N,N-dimethyl-N'-cyclohexylformamidine
Conditions | Yield |
---|---|
at 60℃; | 100% |
In methanol at 25℃; for 12h; | 98% |
1.) 50 deg C, 5 h, 2.) room temperature, 12 h; | 92% |
In benzene for 1h; Heating; | 64% |
dimedone
N,N-dimethyl-formamide dimethyl acetal
2-dimethylaminomethylene-5,5-dimethylcyclohexane-1,3-dione
Conditions | Yield |
---|---|
for 1h; Heating; | 100% |
In 5,5-dimethyl-1,3-cyclohexadiene for 3h; Reflux; | 100% |
at 100℃; for 1h; | 100% |
propylamine
N,N-dimethyl-formamide dimethyl acetal
N2-n-propyl-N1,N1-dimethylformamidine
Conditions | Yield |
---|---|
at 60℃; | 100% |
5-phenyl-cyclohexane-1,3-dione
N,N-dimethyl-formamide dimethyl acetal
2-((dimethylamino)methylene)-5-phenyl-cyclohexane-1,3-dione
Conditions | Yield |
---|---|
for 2h; Reflux; | 100% |
at 100℃; for 1h; | 100% |
for 1h; Heating; | 98% |
3',5'-O-1,1,3,3-tetraisopropyldisiloxan-1,3-diyl-guanosine
N,N-dimethyl-formamide dimethyl acetal
2-N-(Dimethylaminomethylene)-3',5'-O-(tetraisopropyldisiloxane-1,3-diyl)guanosine
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 20h; Ambient temperature; | 100% |
In N,N-dimethyl-formamide at 20℃; for 6h; | 84% |
acetonedicarboxylic acid
N,N-dimethyl-formamide dimethyl acetal
1,5-bis(dimethylamino)-1,4-pentadien-3-one
Conditions | Yield |
---|---|
at 70℃; for 1h; | 100% |
3-(trifluoromethyl)phenylacetone
N,N-dimethyl-formamide dimethyl acetal
1-dimethylamino-2-(m-trifluoromethylphenyl)-1-buten-3-one
Conditions | Yield |
---|---|
for 12h; Heating; | 100% |
hexan-1-amine
N,N-dimethyl-formamide dimethyl acetal
N2-n-hexyl-N1,N1-dimethylformamidine
Conditions | Yield |
---|---|
at 60℃; | 100% |
4-methoxyacetoacetic acid methylester
N,N-dimethyl-formamide dimethyl acetal
methyl 2-[(dimethylamino)methylene]-4-methoxy-3-oxobutanoate
Conditions | Yield |
---|---|
at 20℃; for 24h; | 100% |
at 20℃; for 24h; | 100% |
In N,N-dimethyl-formamide at 120℃; for 0.5h; Inert atmosphere; microwave irradiation; | 97% |
diethyl (2-oxobutyl)phosphonate
N,N-dimethyl-formamide dimethyl acetal
{1-[1-Dimethylamino-meth-(Z)-ylidene]-2-oxo-butyl}-phosphonic acid diethyl ester
Conditions | Yield |
---|---|
With calcium chloride for 2h; Heating; | 100% |
diethyl (2-ethoxycarbonyl)-2-oxoethylphosphonate
N,N-dimethyl-formamide dimethyl acetal
(Z)-3-(Diethoxy-phosphoryl)-4-dimethylamino-2-oxo-but-3-enoic acid ethyl ester
Conditions | Yield |
---|---|
With calcium chloride Ambient temperature; | 100% |
benzyl acetoacetate
N,N-dimethyl-formamide dimethyl acetal
benzyl 2-((dimethylamino)methylene)-3-oxobutanoate
Conditions | Yield |
---|---|
at 20℃; | 100% |
at 20℃; | 100% |
In toluene at 20℃; for 16h; | 100% |
2,6-dinitrotoluene
N,N-dimethyl-formamide dimethyl acetal
3-nitro-trans-2-[β-(dimethylamino)vinyl]-nitrobenzene
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 4h; Heating; | 100% |
In N,N-dimethyl-formamide at 115℃; for 6h; | 96% |
With copper(l) iodide; N,N-dimethyl-formamide at 180℃; under 6000.6 - 7500.75 Torr; for 0.166667h; microwave irradiation; | 85% |
Conditions | Yield |
---|---|
for 21h; Heating; | 100% |
1-methyl-2'-deoxy-5'-O-tritylpseudouridine
N,N-dimethyl-formamide dimethyl acetal
1,3-Dimethyl-2'-deoxy-5'-O-tritylpseudouridine
Conditions | Yield |
---|---|
at 95 - 100℃; for 2h; | 100% |
ethyl 3-(2,3,4,5-tetrafkuorophenyl)-3-oxopropanoate
N,N-dimethyl-formamide dimethyl acetal
ethyl α<(N,N-dimethylamino)methylene>-2,3,4,5-tetrafluoro-β-oxobenzenepropanoate
Conditions | Yield |
---|---|
With acetic anhydride for 0.5h; | 100% |
In toluene at 115 - 120℃; for 1h; | 91% |
2'-O-methyl-5'-O-(dimethoxytrityl)pseudoisocytidine
N,N-dimethyl-formamide dimethyl acetal
N2-<(dimethylamino)methylene>-2'-O-methyl-5'-O-(dimethoxytrityl)pseudoisocytidine
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 5h; Ambient temperature; | 100% |
Methyl 2-oxo-3-phenylthiopropionate
N,N-dimethyl-formamide dimethyl acetal
Methyl 4-dimethylamino-2-oxo-3-phenylthio-3-butenoate
Conditions | Yield |
---|---|
In toluene for 1.5h; Ambient temperature; | 100% |
1-Phenylsulfanyl-3-(2,2,2-trichloro-ethoxy)-propan-2-one
N,N-dimethyl-formamide dimethyl acetal
(Z)-4-Dimethylamino-3-phenylsulfanyl-1-(2,2,2-trichloro-ethoxy)-but-3-en-2-one
Conditions | Yield |
---|---|
at 70℃; for 1.5h; | 100% |
The Molecular Structure of N,N-Dimethylformamide dimethyl acetal (CAS NO.4637-24-5):
Empirical Formula: C5H13NO2
Molecular Weight: 119.1622
IUPAC Name: 1,1-dimethoxy-N,N-dimethylmethanamine
Appearance: clear colourless liquid
Nominal Mass: 119 Da
Average Mass: 119.1622 Da
Monoisotopic Mass: 119.094629 Da
Index of Refraction: 1.407
Molar Refractivity: 32.38 cm3
Molar Volume: 131.4 cm3
Surface Tension: 24.8 dyne/cm
Density: 0.906 g/cm3
Flash Point: 7.2 °C
Enthalpy of Vaporization: 34.33 kJ/mol
Boiling Point: 104.3 °C at 760 mmHg
Vapour Pressure: 31.1 mmHg at 25°C
Storage temp: Fammables area
Water Solubility: hydrolysis
Sensitive: Moisture Sensitive
InChI
InChI=1/C5H13NO2/c1-6(2)5(7-3)8-4/h5H,1-4H3
Smiles
O(C(OC)N(C)C)C
Product Categories: blocks;BuildingBlocks;Aliphatics;(intermediate of zaleplon);Biochemistry;Nucleosides, Nucleotides & Related Reagents;Protecting Agents for Hydroxyl and Amino Groups;Protecting Agents, Phosphorylating Agents & Condensing Agents;Analytical Chemistry;Esterification & Alkylation (GC Derivatizing Reagents);GC Derivatizing Reagents;N,N-Dimethylformamide Dialkylacetals (GC Derivatizing Reagents)
N,N-Dimethylformamide dimethyl acetal (CAS NO.4637-24-5) can be used as intermediates of Zaleplon,also can be used as condensating agent.
Hazard Codes: FXiXn
Risk Statements :
R11: Highly Flammable
R36/37/38: Irritating to eyes, respiratory system and skin
R20/21/22: Harmful by inhalation, in contact with skin and if swallowed
R10: Flammable
Safety Statements :
S16: Keep away from sources of ignition - No smoking
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection
S33: Take precautionary measures against static discharges
S29: Do not empty into drains
S7/9 :Keep container tightly closed and in a well-ventilated place
RIDADR: UN 3271 3/PG 2
N,N-Dimethylformamide dimethyl acetal (CAS NO.4637-24-5) is also called as Dimethylformamide-dimethylacetal ; 1,1-Dimethoxytrimethylamine ; Methanamine, 1,1-dimethoxy-N,N-dimethyl- .
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