phthalimide
potassium phtalimide
Conditions | Yield |
---|---|
With potassium methanolate In ethanol; water at 60 - 65℃; for 13h; Reagent/catalyst; Solvent; Temperature; | 98% |
With potassium hydroxide In ethanol at 75℃; for 1h; | 96% |
With potassium hydroxide In ethanol for 2h; | 91.5% |
Conditions | Yield |
---|---|
With nitrogen at 65℃; for 0.666667h; |
1-bromo-2,2-dimethoxyethane
potassium phtalimide
2-(2,2-dimethoxyethyl)-1H-isoindole-1,3(2H)-dione
Conditions | Yield |
---|---|
With acetamide; potassium iodide at 110 - 140℃; for 3.41667h; | 100% |
In N,N-dimethyl-formamide at 130 - 135℃; for 20h; | 56% |
With acetamide at 170℃; | |
With acetamide; potassium iodide at 130℃; for 5h; |
5-bromopentan-1-nitrile
potassium phtalimide
5-(1,3-dioxoisoindolin-2-yl)pentanenitrile
Conditions | Yield |
---|---|
In DMF (N,N-dimethyl-formamide) at 60℃; for 16h; | 100% |
With ethanol at 120℃; | |
With N,N-dimethyl-formamide | |
In N,N-dimethyl-formamide |
Conditions | Yield |
---|---|
With 18-crown-6 ether In toluene at 100℃; for 6h; | 100% |
at 180℃; | |
With Amberlyst A27 In toluene at 90℃; for 17h; | 100 % Chromat. |
potassium phtalimide
bromopentene
2-(pent-4-enyl)-isoindoline-1,3-dione
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 60℃; for 16h; Gabriel synthesis; Inert atmosphere; | 100% |
In N,N-dimethyl-formamide at 60℃; for 16h; Inert atmosphere; | 100% |
In N,N-dimethyl-formamide at 60℃; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
In 1,1,1-trichloroethane at 60℃; for 24h; | 100% |
In acetone for 24h; Reflux; | 99% |
In acetone for 72h; Reflux; | 91% |
potassium phtalimide
1-bromomethyl-4-bromobenzene
2-(4-bromobenzyl)-1H-isoindole-1,3(2H)-dione
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 100℃; for 6h; | 100% |
In N,N-dimethyl-formamide at 120℃; for 15h; Inert atmosphere; | 82% |
at 200℃; |
potassium phtalimide
p-toluenesulfonyl chloride
N-(4-methylbenzenesulphonyl)phthalimide
Conditions | Yield |
---|---|
With 18-crown-6 ether In benzene at 70℃; for 1h; | 100% |
With 18-crown-6 ether In toluene at 90℃; for 1h; | 100% |
In acetonitrile for 48h; Reflux; | 73% |
at 140℃; | |
In acetonitrile Reflux; |
potassium phtalimide
2-bromomethylnaphthyl bromide
2-[(2-naphthyl)methyl]-1H-isoindole-1,3(2H)-dione
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 120℃; for 15h; Inert atmosphere; | 100% |
at 180℃; | |
In N,N-dimethyl-formamide Alkylation; | |
With tetra-(n-butyl)ammonium iodide In dimethyl sulfoxide for 5h; | |
In N,N-dimethyl-formamide at 50℃; for 2h; |
potassium phtalimide
cinnamyl chloride
2-[(E)-3-phenylprop-2-enyl]-2,3-dihydro-1H-isoindole-1,3-dione
Conditions | Yield |
---|---|
potassium iodide In N,N-dimethyl-formamide at 85 - 90℃; for 8h; | 100% |
at 160℃; |
potassium phtalimide
1-bromomethyl-4-nitro-benzene
2-(4-nitrobenzyl)-1H-isoindole-1,3(2H)-dione
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 2h; | 100% |
In N,N-dimethyl-formamide | 99% |
In N,N-dimethyl-formamide | 99% |
2,3-Dichloro-1,4-naphthoquinone
potassium phtalimide
2,2'-(1,4-dioxo-1,4-dihydronaphthalene-2,3-diyl)bis(isoindoline-1,3-dione)
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 3h; Inert atmosphere; Reflux; | 100% |
In acetonitrile at 85℃; for 3h; | 97% |
In acetonitrile at 85℃; for 3h; | 97% |
Conditions | Yield |
---|---|
[2.2.2]cryptande In tetrahydrofuran for 0.00833333h; | 100% |
In N,N-dimethyl-formamide Heating; | 88% |
With tetrabutylammomium bromide; silica gel for 0.0666667h; microwave irradiation; | 76% |
Conditions | Yield |
---|---|
[2.2.2]cryptande In tetrahydrofuran for 0.25h; | 100% |
N-methyl p-chloro-α-chloroacetanilide
potassium phtalimide
N-phthalimide
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 60 - 75℃; for 2h; room temp. overnight; | 100% |
5-acetylamino-4-methoxy-toluene-2-sulfonyl chloride
potassium phtalimide
Conditions | Yield |
---|---|
With 18-crown-6 ether In toluene at 85℃; for 0.833333h; | 100% |
IUPAC Name: Potassium isoindol-2-ide-1,3-dione
Synonyms of Potassium phthalimide (CAS NO.1074-82-4): Phthalimide potassium ; Phthalimide potassium salt ; N-Potassium phthalimide
Product Categories: Amination; Classes of Metal Compounds; K (Potassium) Compounds (excluding simple potassium salts); N-Substituted Maleimides, Succinimides & Phthalimides; N-Substituted Phthalimides; Synthetic Organic Chemistry; Typical Metal Compounds
CAS NO: 1074-82-4
Molecular Formula: C8H4KNO2
Molecular Weight : 185.2212
Molecular Structure:
EINECS: 214-046-6
H bond acceptors: 3
H bond donors: 1
Freely Rotating Bonds: 0
Polar Surface Area: 49.66Å2
Flash Point: 170.9 °C
Enthalpy of Vaporization: 63.79 kJ/mol
Boiling Point: 359 °C at 760 mmHg
Vapour Pressure: 8.84E-06 mmHg at 25 °C
Melting Point: >300°C
storage temp. Store at RT.
Sensitive Moisture Sensitive
Appearance: Potassium phthalimide (CAS NO.1074-82-4) is slight yellow-green to white powder.
Potassium phthalimide (CAS NO.1074-82-4) is widely used in the production of medicine, pesticide and dye industry.
Hazard Codes: Xi
Risk Statements: 36/37/38
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 22-24/25-26
S22:Do not breathe dust.
S24/25:Avoid contact with skin and eyes.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany: 3
HS Code: 29251995
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