Conditions | Yield |
---|---|
With hydrogenchloride at 0℃; for 0.0833333h; Pinner reaction; Inert atmosphere; | 97% |
With hydrogenchloride; sulfuric acid at -10 - 35℃; for 8h; | 97% |
With acetyl chloride at 0℃; for 12h; Pinner Imino Ether Synthesis; Large scale; | 95% |
ethanol
acetonitrile*2hydrogen chloride
ethyl acetimidate hydrochloride
Conditions | Yield |
---|---|
at -16℃; |
hydrogenchloride
ethanol
acetonitrile
ethyl acetimidate hydrochloride
Conditions | Yield |
---|---|
In methanol; tert-butyl methyl ether at 0℃; for 3.5h; | 13 g |
ethyl acetimidate hydrochloride
methyl 2-amino-6-(ethanimidoylamino)-2-methylhex-4-ynoate
Conditions | Yield |
---|---|
Stage #1: methyl 2,6-diamino-2-methylhex-4-ynoate, dihydrochloride With sodium hydroxide In water at 25℃; for 0.166667h; pH=~ 7.95; Stage #2: ethyl acetimidate hydrochloride With sodium hydroxide In water for 3h; pH=8 - 8.5; Stage #3: With hydrogenchloride In water pH=4.1; | 100% |
Stage #1: methyl 2,6-diamino-2-methylhex-4-ynoate, dihydrochloride; ethyl acetimidate hydrochloride With sodium hydroxide In water for 3.16667h; pH=7.95 - 8.5; Stage #2: With hydrogenchloride In water pH=4.1; | 100% |
tert-butyl (3R,4S)-3,4-diaminopyrrolidine-1-carboxylate
ethyl acetimidate hydrochloride
cis-(3,6)-2-methyl-3a,4,6,6a-tetrahydro-1H-pyrrolo[3.4-d]imidazole-5-carboxylic acid tert-butyl ester
Conditions | Yield |
---|---|
In ethanol at 80℃; for 2.5h; | 100% |
1-amino-4-[(tert-butyloxycarbonyl)amino]butane
ethyl acetimidate hydrochloride
trifluoroacetic acid
Conditions | Yield |
---|---|
Stage #1: 1-amino-4-[(tert-butyloxycarbonyl)amino]butane; ethyl acetimidate hydrochloride With triethylamine at 20℃; Inert atmosphere; Cooling with ice; Stage #2: trifluoroacetic acid | 100% |
ethyl acetimidate hydrochloride
Conditions | Yield |
---|---|
With triethylamine at 5℃; for 2.5h; | 99.1% |
(S,S)-1,2-diaminocyclohexane
ethyl acetimidate hydrochloride
Conditions | Yield |
---|---|
In ethanol at 0 - 20℃; for 8h; Inert atmosphere; | 99% |
In ethanol at 0 - 20℃; | |
In ethanol at 20℃; for 9h; |
ethyl acetimidate hydrochloride
L-cysteine ethyl ester hydrochloride
ethyl 2-methyl-2-thiazoline-(4R)-carboxylate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; | 98% |
With triethylamine In dichloromethane at 0℃; Condensation; | 85% |
ethyl acetimidate hydrochloride
phenylacetyl chloride
ethyl N-phenylacetylacetimidate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 0.5h; | 98% |
(S,S)-1,2-diphenyl-1,2-diaminoethane
ethyl acetimidate hydrochloride
(4S,5S)-2-methyl-4,5-diphenyl-4,5-dihydro-1H-imidazole
Conditions | Yield |
---|---|
In ethanol at 0 - 20℃; for 12h; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
In ethanol Cooling with ice; | 98% |
2-amino-4-(3-fluoro-benzyloxy)-benzoic acid
ethyl acetimidate hydrochloride
7-(3-fluoro-benzyloxy)-2-methyl-3H-quinazolin-4-one
Conditions | Yield |
---|---|
With sodium methylate In methanol for 20h; Heating / reflux; | 97% |
ethyl acetimidate hydrochloride
Conditions | Yield |
---|---|
With potassium carbonate; acetic acid In water; acetonitrile | A n/a B 96% |
Conditions | Yield |
---|---|
With disodium hydrogenphosphate In water at 40℃; for 4h; | 95.3% |
With disodium hydrogenphosphate |
ethyl acetimidate hydrochloride
naphthalene-1-carbonic acid chloride
Naphthalene-1-carboxylic acid [1-ethoxy-eth-(Z)-ylidene]-amide
Conditions | Yield |
---|---|
In toluene for 40h; Ambient temperature; | 95% |
2-amino-2,2-diphenyl-ethanol
ethyl acetimidate hydrochloride
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In chloroform for 12h; Reflux; | 95% |
In dichloromethane at 20℃; | 63% |
Conditions | Yield |
---|---|
Stage #1: ethyl acetimidate hydrochloride With potassium carbonate In dichloromethane; water Stage #2: With acetic acid at 20 - 30℃; for 17.5h; | 95% |
Stage #1: ethyl acetimidate hydrochloride With potassium carbonate Stage #2: With acetic acid | |
Stage #1: ethyl acetimidate hydrochloride With potassium carbonate In dichloromethane; water at 20 - 25℃; Stage #2: With acetic acid at 25℃; for 25h; |
ethyl acetimidate hydrochloride
8-Phenylmenthyl (2S,3S)-3-Amino-2-hydroxy-5-methyl-hexanoate
(4S,5S)-4-Isobutyl-2-methyl-4,5-dihydro-oxazole-5-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
Conditions | Yield |
---|---|
In dichloromethane at 0℃; for 6h; | 94% |
ethyl acetimidate hydrochloride
(-)-8-Phenylmenthyl (2S,3R)-3-Amino-2-hydroxy-5-methyl-hexanoate
(4R,5S)-4-Isobutyl-2-methyl-4,5-dihydro-oxazole-5-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
Conditions | Yield |
---|---|
In dichloromethane at 0℃; for 6h; | 94% |
ethyl acetimidate hydrochloride
cis-4,5-diaminocyclohexene
(3aR,7aS)-2-Methyl-3a,4,7,7a-tetrahydro-1H-benzoimidazole; hydrochloride
Conditions | Yield |
---|---|
In ethanol at 85℃; for 15h; | 93% |
(1R,2S)-2-Amino-1,2-diphenylethanol
ethyl acetimidate hydrochloride
(4S,5R)-2-methyl-4,5-diphenyl-4,5-dihydrooxazole
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 93% |
ethyl acetimidate hydrochloride
N-<β-4-hydroxy-3,5-di-tert-butylphenyl)propionyl>guanidine
2-amino-4-methyl-6-<β-(4-hydroxy-3,5-di-tert-butylphenyl)ethyl>-sym-triazine
Conditions | Yield |
---|---|
In ethanol for 2h; Heating; | 92% |
(R,R)-1,2-diphenylethylenediamine
ethyl acetimidate hydrochloride
(+)-(4R,5R)-2-methyl-4,5-diphenyl-4,5-dihydro-1H-imidazole
Conditions | Yield |
---|---|
In ethanol at 20℃; for 10h; | 92% |
(2S)-2-phenylglycinol
ethyl acetimidate hydrochloride
(4S)-4,5-dihydro-2-methyl-4-phenyl-1,3-oxazole
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 15h; Inert atmosphere; Schlenk technique; | 92% |
In dichloromethane at 20℃; | 68% |
In dichloromethane at 0 - 40℃; for 16h; |
ethyl acetimidate hydrochloride
1-(N-Boc-aminomethyl)-3-(aminomethyl)benzene
Conditions | Yield |
---|---|
In ethanol at 0℃; for 3h; | 92% |
Conditions | Yield |
---|---|
With hydrogenchloride; triethylamine In 1,4-dioxane; ethanol | 92% |
(R)-Phenylglycinol
ethyl acetimidate hydrochloride
(R)-2-methyl-4-phenyl-Δ2-oxazoline
Conditions | Yield |
---|---|
91% | |
Cyclization; |
ethyl acetimidate hydrochloride
p-toluic hydrazide
4-methyl-benzoic acid (1-imino-ethyl)hydrazide
Conditions | Yield |
---|---|
With sodium In ethanol at 20℃; | 91% |
ethyl acetimidate hydrochloride
p-toluic hydrazide
4-methyl-benzoic acid N'-(1-imino-ethyl)-hydrazide
Conditions | Yield |
---|---|
Stage #1: ethyl acetimidate hydrochloride With sodium In ethanol at 20℃; Stage #2: p-toluic hydrazide In ethanol | 91% |
Stage #1: ethyl acetimidate hydrochloride With ethanol; sodium at 20℃; Stage #2: p-toluic hydrazide at 20℃; | 91% |
ethyl acetimidate hydrochloride
methyl (N-(4-chlorophenyl)hydrazono)chloroacetate
1-(4-chlorophenyl)-3-methoxycarbonyl-5-methyl-1,2,4-triazole
Conditions | Yield |
---|---|
With triethylamine In toluene for 2h; Reflux; | 91% |
Molecular Structure of Ethanimidic acid, ethylester, hydrochloride (1:1) (CAS NO.2208-07-3):
IUPAC Name: ethyl ethanimidate hydrochloride
Empirical Formula: C4H10ClNO
Molecular Weight: 123.5813
H bond acceptors: 2
H bond donors: 1
Freely Rotating Bonds: 2
Polar Surface Area: 12.24Å2
Flash Point: 22.3 °C
Enthalpy of Vaporization: 28.76 kJ/mol
Boiling Point: 57.3 °C at 760 mmHg
Vapour Pressure: 232 mmHg at 25°C
Melting point: 112-114 °C(lit.)
Storage temp: 2-8°C
Sensitive: Moisture Sensitive
BRN: 3552401
InChI
InChI=1/C4H9NO.ClH/c1-3-6-4(2)5;/h5H,3H2,1-2H3;1H
Smiles
[NH2+]=C(OCC)C.[ClH-]
EINECS: 218-631-7
Product Categories: Amidates/Imidates; Nitrogen Compounds; Organic Building Blocks
Hazard Codes: Xi
Risk Statements: 36/37/38
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36-37/39
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36:Wear suitable protective clothing.
S37/39:Wear suitable gloves and eye/face protection.
WGK Germany: 3
F: 3-10-21
Ethanimidic acid, ethylester, hydrochloride (1:1) , with CAS number of 2208-07-3, can be called 1-Ethoxyethaniminium chloride ; Ethyl ethanimidoate hydrochloride (1:1) . It is a white to light yellow crystal powder.
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