Product Name

  • Name

    Iminodibenzylcarbonyl chloride

  • EINECS 251-756-5
  • CAS No. 33948-19-5
  • Article Data10
  • CAS DataBase
  • Density 1.282 g/cm3
  • Solubility
  • Melting Point 121-124 °C(lit.)
  • Formula C15H12ClNO
  • Boiling Point 397.5 °C at 760 mmHg
  • Molecular Weight 257.719
  • Flash Point 194.2 °C
  • Transport Information UN 3261 8/PG 2
  • Appearance white to yellowish powder
  • Safety 26-36/37/39-45
  • Risk Codes 34
  • Molecular Structure Molecular Structure of 33948-19-5 (Iminodibenzylcarbonyl chloride)
  • Hazard Symbols CorrosiveC
  • Synonyms 5-(Chlorocarbonyl)-10,11-dihydrodibenzazepine;5-Chlorocarbonyl-10,11-dihydro-5H-dibenz[b,f]azepine;
  • PSA 20.31000
  • LogP 4.34710

Synthetic route

phosgene
75-44-5

phosgene

9,10-dihydrodibenzazepine
494-19-9

9,10-dihydrodibenzazepine

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

Conditions
ConditionsYield
In toluene at 90 - 95℃; for 3.5h;90%
With sodium hydroxide In chlorobenzene at 100 - 115℃; for 4h;80%
With toluene
With toluene
n-butyllithium
109-72-8, 29786-93-4

n-butyllithium

6-fluoro-3-[1-(3-hydroxypropyl)-4-piperidinyl]-1,2-benzisoxazole
150332-87-9

6-fluoro-3-[1-(3-hydroxypropyl)-4-piperidinyl]-1,2-benzisoxazole

A

1-[3-((10,11-dihydro-5H-dibenz[b,f]azepin-5-yl)carbonyloxy)propyl]-4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine, oxalate

1-[3-((10,11-dihydro-5H-dibenz[b,f]azepin-5-yl)carbonyloxy)propyl]-4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine, oxalate

B

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

Conditions
ConditionsYield
In hexane
9,10-dihydrodibenzazepine
494-19-9

9,10-dihydrodibenzazepine

bis(trichloromethyl) carbonate
32315-10-9

bis(trichloromethyl) carbonate

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

Conditions
ConditionsYield
With pyridine In 1,2-dichloro-ethane at 75℃; for 3h; Inert atmosphere;
With sodium hydroxide In chlorobenzene at 100 - 115℃; for 4.5h;
In chlorobenzene at 110℃; for 5h; Temperature;
With sodium hydrogencarbonate In dichloromethane at 0 - 20℃; for 12.5h;
5,10-bis(2-nitrobenzenesulfonyl)-5,10-diaza-1,14-tetradecanediamine
951010-97-2

5,10-bis(2-nitrobenzenesulfonyl)-5,10-diaza-1,14-tetradecanediamine

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

C39H47N7O9S2

C39H47N7O9S2

Conditions
ConditionsYield
In dichloromethane at 20℃; for 19h;95%
In dichloromethane at 20℃;
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

5H-dibenz[b,f]azepine-5-carbonylchloride
33948-22-0

5H-dibenz[b,f]azepine-5-carbonylchloride

Conditions
ConditionsYield
With sodium bromate; N-benzyl-N,N,N-triethylammonium chloride; bromine; dibenzoyl peroxide In chlorobenzene at 92 - 97℃; for 8.5h; Temperature; Reagent/catalyst;90.5%
Multi-step reaction with 2 steps
1: Br2 / chlorobenzene / 1.5 h / 145 - 150 °C
2: chlorobenzene / 2 h / 150 - 155 °C
View Scheme
With bromine In chlorobenzene at 80℃; for 6h; Temperature; Inert atmosphere;
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

9,10-dihydrodibenzazepine
494-19-9

9,10-dihydrodibenzazepine

Conditions
ConditionsYield
In acetonitrile electrolysis (Et4NClO4, Hg-dropelectrode);90%
Methyl-(1-methyl-[4]piperidyl)-amin
73579-08-5

Methyl-(1-methyl-[4]piperidyl)-amin

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

N-methyl-N-(1-methylpiperodin-4-yl)-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide

N-methyl-N-(1-methylpiperodin-4-yl)-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide

Conditions
ConditionsYield
With triethylamine In dichloromethane for 2h; Heating;90%
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

10,11-Dihydrocarbamazepin
3564-73-6

10,11-Dihydrocarbamazepin

Conditions
ConditionsYield
With ammonia In methanol; water at 57 - 59℃; for 1.5h;85.35%
With ethanol; ammonia
With ethanol; ammonia
pyrrolidine
123-75-1

pyrrolidine

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

(10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)(pyrrolidin-1-yl)methanone
294194-09-5

(10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)(pyrrolidin-1-yl)methanone

Conditions
ConditionsYield
With triethylamine In benzene85%
4-phenyl-1-piperazine
92-54-6

4-phenyl-1-piperazine

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

(11,12-dihydro-5H-dibenzo[b,f]azepin-5-yl)(4-phenylpiperazin-1-yl)methanone
1250430-98-8

(11,12-dihydro-5H-dibenzo[b,f]azepin-5-yl)(4-phenylpiperazin-1-yl)methanone

Conditions
ConditionsYield
With triethylamine In 1,4-dioxane83%
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

Propargylamine
2450-71-7

Propargylamine

N-(prop-2-ynyl)-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide
127025-48-3

N-(prop-2-ynyl)-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃; for 24h; Reflux;76%
1-phenylmethylpiperazine
2759-28-6

1-phenylmethylpiperazine

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

5-[(4-benzylpiperazin-1-yl)carbonyl]-10,11-dihydro-5H-dibenzo[b,f]azepine

5-[(4-benzylpiperazin-1-yl)carbonyl]-10,11-dihydro-5H-dibenzo[b,f]azepine

Conditions
ConditionsYield
With triethylamine In dichloromethane for 2h; Heating;75%
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

methyl 3,5-diaminobenzoate
1949-55-9

methyl 3,5-diaminobenzoate

N,N'-bis(iminodibenzyl-5-carbonyl)-3,5-diaminobenzoic methyl ester
175085-87-7

N,N'-bis(iminodibenzyl-5-carbonyl)-3,5-diaminobenzoic methyl ester

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane for 24h; Heating;72%
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

2-propynyl 3-hydroxy-9β,13α-dimethyl-2-oxo-24,25,26-trinoroleana-1(10),3,5,7-tetraen-29-oate

2-propynyl 3-hydroxy-9β,13α-dimethyl-2-oxo-24,25,26-trinoroleana-1(10),3,5,7-tetraen-29-oate

(6bS,8aS,11R,12bS,14aR)-4,6b,8a,11,12b,14a-hexamethyl-2-oxo-11-((prop-2-yn-1-yloxy)carbonyl)-2,6b,7,8,8a,9,10,11,12,12a,12b,13,14,14a-tetradecahydropicen-3-yl 10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxylate

(6bS,8aS,11R,12bS,14aR)-4,6b,8a,11,12b,14a-hexamethyl-2-oxo-11-((prop-2-yn-1-yloxy)carbonyl)-2,6b,7,8,8a,9,10,11,12,12a,12b,13,14,14a-tetradecahydropicen-3-yl 10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxylate

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane at 0 - 25℃; for 12h;62%
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

(2S)-2-[(10,11-dihydro-5H-dibenzo[b,f]azepin-5-ylcarbonyl)amino]-3-(1H-indol-3-yl)propionic acid methyl ester

(2S)-2-[(10,11-dihydro-5H-dibenzo[b,f]azepin-5-ylcarbonyl)amino]-3-(1H-indol-3-yl)propionic acid methyl ester

Conditions
ConditionsYield
With N-ethylmorpholine; In N,N-dimethyl-formamide at 0 - 40℃;30.3%
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

N,N',N'-trimethylenediamine
142-25-6

N,N',N'-trimethylenediamine

10,11-dihydro-dibenz[b,f]azepine-5-carboxylic acid-[(2-dimethylamino-ethyl)-methyl-amide]

10,11-dihydro-dibenz[b,f]azepine-5-carboxylic acid-[(2-dimethylamino-ethyl)-methyl-amide]

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

10-bromo-10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-20-8

10-bromo-10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

Conditions
ConditionsYield
With bromine In chlorobenzene at 145 - 150℃; for 1.5h;
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

NG-tosylargine
4353-32-6

NG-tosylargine

Nα-(10,11-dihydroo-5H-dibenz[b.f]azepine-5-carbonyl)toluenesulfonyl-L-arginine

Nα-(10,11-dihydroo-5H-dibenz[b.f]azepine-5-carbonyl)toluenesulfonyl-L-arginine

Conditions
ConditionsYield
With sodium carbonate In 1,4-dioxane
Spermine
71-44-3

Spermine

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

C25H37N5O

C25H37N5O

Conditions
ConditionsYield
In dichloromethane at 20℃;
C23H34N6O8S2
951010-96-1

C23H34N6O8S2

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

C38H45N7O9S2

C38H45N7O9S2

Conditions
ConditionsYield
In dichloromethane at 20℃;
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

carbamazepin
298-46-4

carbamazepin

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: Br2 / chlorobenzene / 1.5 h / 145 - 150 °C
2: chlorobenzene / 2 h / 150 - 155 °C
3: 25percent NH4OH / methanol / 5 h / 75 - 85 °C
View Scheme
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

(S)-1-(10,11-Dihydro-5H-dibenz[b,f]azepine-5-carbonyl)-4-(benzyloxycarbonyl)piperazine-2-carboxylic acid

(S)-1-(10,11-Dihydro-5H-dibenz[b,f]azepine-5-carbonyl)-4-(benzyloxycarbonyl)piperazine-2-carboxylic acid

Conditions
ConditionsYield
284 mg (24%)
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

benzylamine
100-46-9

benzylamine

10,11-dihydro-dibenzo[b,f]azepine-5-carboxylic acid benzylamide

10,11-dihydro-dibenzo[b,f]azepine-5-carboxylic acid benzylamide

Conditions
ConditionsYield
In dichloromethane at 20℃; for 27h;
C17H22N2O3*ClH
1131679-43-0

C17H22N2O3*ClH

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

C32H33N3O4
1131680-29-9

C32H33N3O4

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran
C17H22N2O3*ClH
1131679-47-4

C17H22N2O3*ClH

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

C32H33N3O4
1131680-31-3

C32H33N3O4

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

10,11-Dihydro-dibenzo[b,f]azepine-5-carboxylic acid hydrazide
1676-31-9

10,11-Dihydro-dibenzo[b,f]azepine-5-carboxylic acid hydrazide

Conditions
ConditionsYield
With hydrazine hydrate In diethyl ether; ethanol for 0.5h; Schlenk technique; Inert atmosphere;
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

[ReBr(CO)3(H2BF)]
1417342-96-1

[ReBr(CO)3(H2BF)]

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: hydrazine hydrate / diethyl ether; ethanol / 0.5 h / Schlenk technique; Inert atmosphere
2: toluene-4-sulfonic acid / toluene / 0.5 h / 20 °C / Schlenk technique; Inert atmosphere
3: toluene / 5 h / Schlenk technique; Inert atmosphere; Reflux
View Scheme
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

C22H19N3O2
1417342-90-5

C22H19N3O2

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: hydrazine hydrate / diethyl ether; ethanol / 0.5 h / Schlenk technique; Inert atmosphere
2: toluene-4-sulfonic acid / toluene / 0.5 h / 20 °C / Schlenk technique; Inert atmosphere
View Scheme
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

(R)-Phenylglycinol
56613-80-0

(R)-Phenylglycinol

C23H22N2O2

C23H22N2O2

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃; for 12h; Inert atmosphere;
10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride
33948-19-5

10,11-dihydro-dibenzo[b,f]azepine-5-carbonyl chloride

(R)-Phenylglycinol
56613-80-0

(R)-Phenylglycinol

C33H43N3O6Si

C33H43N3O6Si

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: triethylamine / dichloromethane / 12 h / 0 °C / Inert atmosphere
2: triethylamine / benzene / 72 h / 111 °C / Inert atmosphere
View Scheme

Iminodibenzylcarbonyl chloride Chemical Properties

Molecular Structure:

Molecular Formula: C15H12ClNO
Molecular Weight: 257.7149
IUPAC Name: 5,6-Dihydrobenzo[b][1]benzazepine-11-carbonyl chloride
Synonyms of Iminodibenzylcarbonyl chloride (CAS NO.33948-19-5): EINECS 251-756-5 ; 10,11-Dihydro-5H-dibenz(b,f)azepine-5-carbonyl chloride
CAS NO: 33948-19-5
Product Categories: (intermediate of carbamazepine)
Melting point: 121-124 °C 
Index of Refraction: 1.628
Molar Refractivity: 71.39 cm3
Molar Volume: 200.9 cm3
Surface Tension: 50.1 dyne/cm
Density: 1.282 g/cm3
Flash Point: 194.2 °C
Enthalpy of Vaporization: 64.79 kJ/mol
Boiling Point: 397.5 °C at 760 mmHg
Vapour Pressure: 1.58E-06 mmHg at 25°C

Iminodibenzylcarbonyl chloride Uses

 Iminodibenzylcarbonyl chloride (CAS NO.33948-19-5) is used as pharmaceutical intermediates.

Iminodibenzylcarbonyl chloride Safety Profile

Hazard Codes of Iminodibenzylcarbonyl chloride (CAS NO.33948-19-5): CorrosiveC
Risk Statements: 34 
R34: Causes burns.
Safety Statements: 26-36/37/39-45 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection. 
S45: In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
RIDADR: UN 3261 8/PG 2
WGK Germany: 3
HazardClass: 8
PackingGroup: III

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