Product Name

  • Name

    Ethyl acetimidate hydrochloride

  • EINECS 218-631-7
  • CAS No. 2208-07-3
  • Article Data38
  • CAS DataBase
  • Density 0.89g/cm3
  • Solubility Soluble in water (50mg/L).
  • Melting Point 112-114 °C(lit.)
  • Formula C4H10ClNO
  • Boiling Point 57.3 °C at 760 mmHg
  • Molecular Weight 123.582
  • Flash Point 22.3 °C
  • Transport Information
  • Appearance white to light yellow crystal powder
  • Safety 26-36-37/39
  • Risk Codes 36/37/38
  • Molecular Structure Molecular Structure of 2208-07-3 (Ethyl acetimidate hydrochloride)
  • Hazard Symbols IrritantXi
  • Synonyms Acetimidicacid, ethyl ester, hydrochloride (6CI,7CI,8CI);Ethanimidic acid, ethyl ester,hydrochloride (9CI);Ethyl acetoamidatehydrochloride;Ethyl acetocarboximidate hydrochloride;Ethyl acetoimidatehydrochloride;Ethyl ethanimidate hydrochloride;Ethyl iminoacetatehydrochloride;
  • PSA 33.08000
  • LogP 1.92180

Synthetic route

ethanol
64-17-5

ethanol

acetonitrile
75-05-8

acetonitrile

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

Conditions
ConditionsYield
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
64-17-5

ethanol

acetonitrile*2hydrogen chloride
73233-19-9, 90586-61-1

acetonitrile*2hydrogen chloride

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

Conditions
ConditionsYield
at -16℃;
acetamide
60-35-5

acetamide

chloroformic acid ethyl ester
541-41-3

chloroformic acid ethyl ester

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

hydrogenchloride
7647-01-0

hydrogenchloride

ethanol
64-17-5

ethanol

acetonitrile
75-05-8

acetonitrile

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

acetyl chloride
75-36-5

acetyl chloride

acetonitrile
75-05-8

acetonitrile

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

Conditions
ConditionsYield
In methanol; tert-butyl methyl ether at 0℃; for 3.5h;13 g
methyl 2,6-diamino-2-methylhex-4-ynoate, dihydrochloride

methyl 2,6-diamino-2-methylhex-4-ynoate, dihydrochloride

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

methyl 2-amino-6-(ethanimidoylamino)-2-methylhex-4-ynoate
404860-60-2

methyl 2-amino-6-(ethanimidoylamino)-2-methylhex-4-ynoate

Conditions
ConditionsYield
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
945217-60-7

tert-butyl (3R,4S)-3,4-diaminopyrrolidine-1-carboxylate

ethyl acetimidate hydrochloride
2208-07-3

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
1202067-52-4

cis-(3,6)-2-methyl-3a,4,6,6a-tetrahydro-1H-pyrrolo[3.4-d]imidazole-5-carboxylic acid tert-butyl ester

Conditions
ConditionsYield
In ethanol at 80℃; for 2.5h;100%
1-amino-4-[(tert-butyloxycarbonyl)amino]butane
68076-36-8

1-amino-4-[(tert-butyloxycarbonyl)amino]butane

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

trifluoroacetic acid
76-05-1

trifluoroacetic acid

tert-butyl N-[4-(ethanimidoylamino)butyl]carbamate trifluoroacetate

tert-butyl N-[4-(ethanimidoylamino)butyl]carbamate trifluoroacetate

Conditions
ConditionsYield
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
2208-07-3

ethyl acetimidate hydrochloride

ethyl (2S)-3-(7-amidino-2-naphthyl)-2-<4-<(3S)-3-pyrrolidinyloxy>phenyl>propanoate dihydrochloride

ethyl (2S)-3-(7-amidino-2-naphthyl)-2-<4-<(3S)-3-pyrrolidinyloxy>phenyl>propanoate dihydrochloride

ethyl (2S)-2-<4-<<(3S)-1-acetimidoyl-3-pyrrolidinyl>oxy>phenyl>3-(7-amidino-2-naphthyl)propanoate dihydrochloride

ethyl (2S)-2-<4-<<(3S)-1-acetimidoyl-3-pyrrolidinyl>oxy>phenyl>3-(7-amidino-2-naphthyl)propanoate dihydrochloride

Conditions
ConditionsYield
With triethylamine at 5℃; for 2.5h;99.1%
(S,S)-1,2-diaminocyclohexane
21436-03-3

(S,S)-1,2-diaminocyclohexane

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

(3aS,7aS)-2-methyl-3a,4,5,6,7,7a-hexahydro-1H-benzo[d]imidazole

(3aS,7aS)-2-methyl-3a,4,5,6,7,7a-hexahydro-1H-benzo[d]imidazole

Conditions
ConditionsYield
In ethanol at 0 - 20℃; for 8h; Inert atmosphere;99%
In ethanol at 0 - 20℃;
In ethanol at 20℃; for 9h;
ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

L-cysteine ethyl ester hydrochloride
868-59-7

L-cysteine ethyl ester hydrochloride

ethyl 2-methyl-2-thiazoline-(4R)-carboxylate
89530-18-7

ethyl 2-methyl-2-thiazoline-(4R)-carboxylate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃;98%
With triethylamine In dichloromethane at 0℃; Condensation;85%
ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

phenylacetyl chloride
103-80-0

phenylacetyl chloride

ethyl N-phenylacetylacetimidate
107465-70-3

ethyl N-phenylacetylacetimidate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 0.5h;98%
(S,S)-1,2-diphenyl-1,2-diaminoethane
29841-69-8

(S,S)-1,2-diphenyl-1,2-diaminoethane

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

(4S,5S)-2-methyl-4,5-diphenyl-4,5-dihydro-1H-imidazole
109830-48-0, 133815-21-1

(4S,5S)-2-methyl-4,5-diphenyl-4,5-dihydro-1H-imidazole

Conditions
ConditionsYield
In ethanol at 0 - 20℃; for 12h; Inert atmosphere;98%
ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

C14H22N2O

C14H22N2O

C16H25N3O*ClH

C16H25N3O*ClH

Conditions
ConditionsYield
In ethanol Cooling with ice;98%
2-amino-4-(3-fluoro-benzyloxy)-benzoic acid
713511-21-8

2-amino-4-(3-fluoro-benzyloxy)-benzoic acid

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

7-(3-fluoro-benzyloxy)-2-methyl-3H-quinazolin-4-one
713511-22-9

7-(3-fluoro-benzyloxy)-2-methyl-3H-quinazolin-4-one

Conditions
ConditionsYield
With sodium methylate In methanol for 20h; Heating / reflux;97%
3-amino-5-ethyl-4-(3-pentyl)pyrazole

3-amino-5-ethyl-4-(3-pentyl)pyrazole

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

A

3-acetamidino-5-ethyl-4-(3-pentyl)pyrazole, hydrochloride salt

3-acetamidino-5-ethyl-4-(3-pentyl)pyrazole, hydrochloride salt

B

4-phenyl-8-(3-pentyl)-7-ethyl-2-methyl-pyrazolo[1,5-a]-1,3,5-triazine

4-phenyl-8-(3-pentyl)-7-ethyl-2-methyl-pyrazolo[1,5-a]-1,3,5-triazine

Conditions
ConditionsYield
With potassium carbonate; acetic acid In water; acetonitrileA n/a
B 96%
CYANAMID
420-04-2

CYANAMID

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

ethyl N‐cyanoethanimidate
1558-82-3

ethyl N‐cyanoethanimidate

Conditions
ConditionsYield
With disodium hydrogenphosphate In water at 40℃; for 4h;95.3%
With disodium hydrogenphosphate
ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

naphthalene-1-carbonic acid chloride
879-18-5

naphthalene-1-carbonic acid chloride

Naphthalene-1-carboxylic acid [1-ethoxy-eth-(Z)-ylidene]-amide
130168-80-8

Naphthalene-1-carboxylic acid [1-ethoxy-eth-(Z)-ylidene]-amide

Conditions
ConditionsYield
In toluene for 40h; Ambient temperature;95%
2-amino-2,2-diphenyl-ethanol
18903-44-1

2-amino-2,2-diphenyl-ethanol

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

4,4-diphenyl-2-methyl-1,3-oxazolin

4,4-diphenyl-2-methyl-1,3-oxazolin

Conditions
ConditionsYield
With lithium aluminium tetrahydride In chloroform for 12h; Reflux;95%
In dichloromethane at 20℃;63%
ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

2,4,6-trimethyl-s-triazine
823-94-9

2,4,6-trimethyl-s-triazine

Conditions
ConditionsYield
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
2208-07-3

ethyl acetimidate hydrochloride

8-Phenylmenthyl (2S,3S)-3-Amino-2-hydroxy-5-methyl-hexanoate
128162-92-5

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
128162-93-6

(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
ConditionsYield
In dichloromethane at 0℃; for 6h;94%
ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

(-)-8-Phenylmenthyl (2S,3R)-3-Amino-2-hydroxy-5-methyl-hexanoate
128114-54-5

(-)-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
128114-55-6

(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
ConditionsYield
In dichloromethane at 0℃; for 6h;94%
ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

cis-4,5-diaminocyclohexene
129884-37-3, 782445-78-7

cis-4,5-diaminocyclohexene

(3aR,7aS)-2-Methyl-3a,4,7,7a-tetrahydro-1H-benzoimidazole; hydrochloride
129884-40-8

(3aR,7aS)-2-Methyl-3a,4,7,7a-tetrahydro-1H-benzoimidazole; hydrochloride

Conditions
ConditionsYield
In ethanol at 85℃; for 15h;93%
(1R,2S)-2-Amino-1,2-diphenylethanol
23190-16-1

(1R,2S)-2-Amino-1,2-diphenylethanol

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

(4S,5R)-2-methyl-4,5-diphenyl-4,5-dihydrooxazole
474669-82-4

(4S,5R)-2-methyl-4,5-diphenyl-4,5-dihydrooxazole

Conditions
ConditionsYield
In dichloromethane at 20℃;93%
ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

N-<β-4-hydroxy-3,5-di-tert-butylphenyl)propionyl>guanidine
114811-78-8

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
114811-79-9

2-amino-4-methyl-6-<β-(4-hydroxy-3,5-di-tert-butylphenyl)ethyl>-sym-triazine

Conditions
ConditionsYield
In ethanol for 2h; Heating;92%
(R,R)-1,2-diphenylethylenediamine
35132-20-8

(R,R)-1,2-diphenylethylenediamine

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

(+)-(4R,5R)-2-methyl-4,5-diphenyl-4,5-dihydro-1H-imidazole
320778-88-9

(+)-(4R,5R)-2-methyl-4,5-diphenyl-4,5-dihydro-1H-imidazole

Conditions
ConditionsYield
In ethanol at 20℃; for 10h;92%
(2S)-2-phenylglycinol
20989-17-7

(2S)-2-phenylglycinol

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

(4S)-4,5-dihydro-2-methyl-4-phenyl-1,3-oxazole
222622-39-1

(4S)-4,5-dihydro-2-methyl-4-phenyl-1,3-oxazole

Conditions
ConditionsYield
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
2208-07-3

ethyl acetimidate hydrochloride

1-(N-Boc-aminomethyl)-3-(aminomethyl)benzene
108467-99-8

1-(N-Boc-aminomethyl)-3-(aminomethyl)benzene

N-(3-(N-Boc-aminomethyl)benzyl)acetimidine hydrochloride

N-(3-(N-Boc-aminomethyl)benzyl)acetimidine hydrochloride

Conditions
ConditionsYield
In ethanol at 0℃; for 3h;92%
ethyl N-[3-(3-amidinophenyl)-2-(E)-propenyl]-N-[5-carbamoyl-2-methyl-4-(piperidin-4-yloxy)phenyl]sulfamoylacetate dihydrochloride

ethyl N-[3-(3-amidinophenyl)-2-(E)-propenyl]-N-[5-carbamoyl-2-methyl-4-(piperidin-4-yloxy)phenyl]sulfamoylacetate dihydrochloride

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

acetonitrile
75-05-8

acetonitrile

Ethyl N-[4-(1-acetimidoylpiperidin-4-yloxy)-5-carbamoyl-2-methylphenyl]-N-[3-(3-amidinophenyl)-2-(E)-propenyl]sulfamoylacetate dihydrochloride

Ethyl N-[4-(1-acetimidoylpiperidin-4-yloxy)-5-carbamoyl-2-methylphenyl]-N-[3-(3-amidinophenyl)-2-(E)-propenyl]sulfamoylacetate dihydrochloride

Conditions
ConditionsYield
With hydrogenchloride; triethylamine In 1,4-dioxane; ethanol92%
(R)-Phenylglycinol
56613-80-0

(R)-Phenylglycinol

ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

(R)-2-methyl-4-phenyl-Δ2-oxazoline
116173-81-0

(R)-2-methyl-4-phenyl-Δ2-oxazoline

Conditions
ConditionsYield
91%
Cyclization;
ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

p-toluic hydrazide
3619-22-5

p-toluic hydrazide

4-methyl-benzoic acid (1-imino-ethyl)hydrazide
1314991-79-1

4-methyl-benzoic acid (1-imino-ethyl)hydrazide

Conditions
ConditionsYield
With sodium In ethanol at 20℃;91%
ethyl acetimidate hydrochloride
2208-07-3

ethyl acetimidate hydrochloride

p-toluic hydrazide
3619-22-5

p-toluic hydrazide

4-methyl-benzoic acid N'-(1-imino-ethyl)-hydrazide
210179-03-6

4-methyl-benzoic acid N'-(1-imino-ethyl)-hydrazide

Conditions
ConditionsYield
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
2208-07-3

ethyl acetimidate hydrochloride

methyl (N-(4-chlorophenyl)hydrazono)chloroacetate
62465-90-1

methyl (N-(4-chlorophenyl)hydrazono)chloroacetate

1-(4-chlorophenyl)-3-methoxycarbonyl-5-methyl-1,2,4-triazole
933221-18-2

1-(4-chlorophenyl)-3-methoxycarbonyl-5-methyl-1,2,4-triazole

Conditions
ConditionsYield
With triethylamine In toluene for 2h; Reflux;91%

Ethyl acetimidate hydrochloride Chemical Properties

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

Ethyl acetimidate hydrochloride Safety Profile

Hazard Codes: IrritantXi
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

Ethyl acetimidate hydrochloride Specification

 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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