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6293-01-2

Basic Information
CAS No.: 6293-01-2
Name: Iso Methadone
Article Data: 17
Molecular Structure:
Molecular Structure of 6293-01-2 (Iso Methadone)
Formula: C19H22 N2
Molecular Weight: 278.397
Synonyms: Butyronitrile,4-(dimethylamino)-3-methyl-2,2-diphenyl- (6CI,7CI,8CI);2,2-Diphenyl-3-methyl-4-(dimethylamino)butyronitrile; NSC 9993; Tuso-Blandin
Density: 1.032g/cm3
Melting Point: 66-67 °C
Boiling Point: 402.9°Cat760mmHg
Flash Point: 165.9°C
PSA: 27.03000
LogP: 3.69398
Synthetic route
86-29-3

Diphenylacetonitrile

108-14-5

2-chloro-1-dimethylaminopropane

A

125-79-1

(R,S)-2,2-diphenyl-4-dimethylaminopentanenitrile

B

6293-01-2

2,2-diphenyl-3-methyl-4-(dimethylamino)-butyronitrile

Conditions
ConditionsYield
With sodium hydroxide In N,N-dimethyl-formamide at 75 - 80℃; for 1h; Inert atmosphere;A 45%
B n/a
With potassium tert-butylate Title compound not separated from byproducts;
With potassium tert-butylate
86-29-3

Diphenylacetonitrile

A

125-79-1

(R,S)-2,2-diphenyl-4-dimethylaminopentanenitrile

B

6293-01-2

2,2-diphenyl-3-methyl-4-(dimethylamino)-butyronitrile

Conditions
ConditionsYield
With lithium amide; benzene Erwaermen des Reaktionsgemisches mit (+-)-Dimethyl-<2-chlor-propyl>-amin;
With sodium amide; benzene Erwaermen des Reaktionsgemisches mit (+-)-Dimethyl-<2-chlor-propyl>-amin;
With xylene; sodium t-butanolate; tert-butyl alcohol Erwaermen des Reaktionsgemisches mit (+-)-Dimethyl-<2-chlor-propyl>-amin;
56-23-5

tetrachloromethane

86-29-3

Diphenylacetonitrile

865-47-4

potassium tert-butylate

53309-35-6

(2-chloro-1-methyl-ethyl)-dimethyl-amine

A

125-79-1

(R,S)-2,2-diphenyl-4-dimethylaminopentanenitrile

B

6293-01-2

2,2-diphenyl-3-methyl-4-(dimethylamino)-butyronitrile

56-23-5

tetrachloromethane

86-29-3

Diphenylacetonitrile

865-47-4

potassium tert-butylate

75-65-0

tert-butyl alcohol

A

125-79-1

(R,S)-2,2-diphenyl-4-dimethylaminopentanenitrile

B

6293-01-2

2,2-diphenyl-3-methyl-4-(dimethylamino)-butyronitrile

Conditions
ConditionsYield
bei Siedetemperatur; Erwaermen des Reaktionsgemisches mit (+-)-Dimethyl-<2-chlor-propyl>-amin;
86-29-3

Diphenylacetonitrile

4584-49-0

(2-chloropropyl)dimethylamine hydrochloride

A

125-79-1

(R,S)-2,2-diphenyl-4-dimethylaminopentanenitrile

B

6293-01-2

2,2-diphenyl-3-methyl-4-(dimethylamino)-butyronitrile

Conditions
ConditionsYield
With sodium hydroxide; dibenzo-18-crown-6 1.) DMSO, water; 2.) 45 deg C, 2 h; Yield given. Multistep reaction. Yields of byproduct given;
Stage #1: Diphenylacetonitrile With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride In dimethyl sulfoxide for 0.25h;
Stage #2: (2-chloropropyl)dimethylamine hydrochloride In dimethyl sulfoxide at 40℃; for 1h;
56-23-5

tetrachloromethane

108-14-5

2-chloro-1-dimethylaminopropane

75-65-0

tert-butyl alcohol

potassium diphenylacetonitrile

potassium diphenylacetonitrile

A

125-79-1

(R,S)-2,2-diphenyl-4-dimethylaminopentanenitrile

B

6293-01-2

2,2-diphenyl-3-methyl-4-(dimethylamino)-butyronitrile

108-14-5

2-chloro-1-dimethylaminopropane

71-43-2

benzene

potassium diphenylacetonitrile

potassium diphenylacetonitrile

A

125-79-1

(R,S)-2,2-diphenyl-4-dimethylaminopentanenitrile

B

6293-01-2

2,2-diphenyl-3-methyl-4-(dimethylamino)-butyronitrile

56-23-5

tetrachloromethane

108-14-5

2-chloro-1-dimethylaminopropane

75-65-0

tert-butyl alcohol

sodium diphenylacetonitrile

sodium diphenylacetonitrile

A

125-79-1

(R,S)-2,2-diphenyl-4-dimethylaminopentanenitrile

B

6293-01-2

2,2-diphenyl-3-methyl-4-(dimethylamino)-butyronitrile

108-14-5

2-chloro-1-dimethylaminopropane

71-43-2

benzene

sodium diphenylacetonitrile

sodium diphenylacetonitrile

A

125-79-1

(R,S)-2,2-diphenyl-4-dimethylaminopentanenitrile

B

6293-01-2

2,2-diphenyl-3-methyl-4-(dimethylamino)-butyronitrile

86-29-3

Diphenylacetonitrile

sodium amide

71-43-2

benzene

A

125-79-1

(R,S)-2,2-diphenyl-4-dimethylaminopentanenitrile

B

6293-01-2

2,2-diphenyl-3-methyl-4-(dimethylamino)-butyronitrile

Conditions
ConditionsYield
Erwaermen des Reaktionsgemisches mit (+-)-Dimethyl-<2-chlor-propyl>-amin;
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