1-(dimethylamino)cyclohexanecarbonitrile
1-aminomethyl‐1‐cyclohexanedimethylamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether; water at 20℃; | 92.5% |
With lithium aluminium tetrahydride; sulfuric acid In tetrahydrofuran at 40 - 50℃; for 1h; | 66% |
With lithium aluminium tetrahydride; sulfuric acid In tetrahydrofuran at 0 - 20℃; for 18h; | |
With lithium aluminium tetrahydride In diethyl ether at 20℃; for 16h; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: H2O / 18 h 2: LiAlH4; H2SO4 / tetrahydrofuran / 18 h / 0 - 20 °C View Scheme |
cyclohexanone
1-aminomethyl‐1‐cyclohexanedimethylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 85 percent / H2O / Ambient temperature 2: 66 percent / LiAlH4, H2SO4 / tetrahydrofuran / 1 h / 40 - 50 °C View Scheme |
cyclohexanone
1-aminomethyl‐1‐cyclohexanedimethylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: hydrogenchloride / water / 16 h / 20 °C 2: lithium aluminium tetrahydride / diethyl ether / 16 h / 20 °C View Scheme |
1-aminomethyl‐1‐cyclohexanedimethylamine
4-(benzyloxy)-3,5-dimethoxybenzoic acid
Conditions | Yield |
---|---|
Stage #1: 1-aminomethyl‐1‐cyclohexanedimethylamine; 4-(benzyloxy)-3,5-dimethoxybenzoic acid With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 0 - 20℃; for 24h; Stage #2: With hydrogenchloride In methanol | 55.5% |
1-aminomethyl‐1‐cyclohexanedimethylamine
C11H12ClNO5
Conditions | Yield |
---|---|
In tetrahydrofuran Ambient temperature; |
4-butoxy-3,5-dimethoxybenzoic acid chloride
1-aminomethyl‐1‐cyclohexanedimethylamine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran |
1-aminomethyl‐1‐cyclohexanedimethylamine
4-chloro-benzoyl chloride
Conditions | Yield |
---|---|
In chloroform; water; benzene |
1-aminomethyl‐1‐cyclohexanedimethylamine
benzoyl chloride
1-benzamidomethylcyclohexyldimethylamine hydrochloride
Conditions | Yield |
---|---|
With pyridine |
1-aminomethyl‐1‐cyclohexanedimethylamine
3,4-dimethoxybenzoic acid chloride
Conditions | Yield |
---|---|
In water; benzene |
1-aminomethyl‐1‐cyclohexanedimethylamine
o-chlorobenzoyl chloride
B
2-chlorobenzamido-methyl-cyclohexyl-dimethylamine hydrochloride
Conditions | Yield |
---|---|
In benzene |
1-aminomethyl‐1‐cyclohexanedimethylamine
3,4-dichlorobenzoyl chloride
Conditions | Yield |
---|---|
With pyridine |
1-aminomethyl‐1‐cyclohexanedimethylamine
4-methyl-benzoyl chloride
Conditions | Yield |
---|---|
With triethylamine In water; benzene |
1-aminomethyl‐1‐cyclohexanedimethylamine
acetamidomethylcyclohexyl-dimethylamine
Conditions | Yield |
---|---|
With sodium hydroxide; acetic anhydride; sodium carbonate |
4-{[2-(isopropylsulfonyl)phenyl]amino}-2-(methylsulfanyl)-6-oxo-1,6-dihydropyrimidine-5-carboxamide
1-aminomethyl‐1‐cyclohexanedimethylamine
2-({[1-(dimethylamino)cyclohexyl]methyl}amino)-4-{[2-(isopropylsulfonyl)phenyl]amino}-6-oxo-1,6-dihydropyrimidine-5-carboxamide
Conditions | Yield |
---|---|
In 1-methyl-pyrrolidin-2-one at 180℃; for 0.166667h; Microwave irradiation; |
1-aminomethyl‐1‐cyclohexanedimethylamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: triethylamine / tetrahydrofuran / 1 h / 20 °C 1.2: 1 h / 20 °C 2.1: diethylazodicarboxylate / toluene / 18 h / 55 °C View Scheme |
1-aminomethyl‐1‐cyclohexanedimethylamine
3,4-dichlorobenzoyl chloride
AH 7921
Conditions | Yield |
---|---|
Stage #1: 1-aminomethyl‐1‐cyclohexanedimethylamine With triethylamine In tetrahydrofuran at 20℃; for 1h; Stage #2: 3,4-dichlorobenzoyl chloride In tetrahydrofuran at 20℃; for 1h; | 30.65 g |
With triethylamine In diethyl ether at 20℃; for 16h; |
1-aminomethyl‐1‐cyclohexanedimethylamine
Conditions | Yield |
---|---|
In tetrahydrofuran Reflux; |
1-aminomethyl‐1‐cyclohexanedimethylamine
4-chloro-benzoyl chloride
4-Chlorbenzamidomethylcyclohexyldimethylamin
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 20℃; for 16h; |
1-aminomethyl‐1‐cyclohexanedimethylamine
4-trifluoromethyl-phenyl acetyl chloride
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 20℃; for 16h; |
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