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Home > Encyclopedia > 2-Chloro-1,3-dimethylimidazolidinium chloride

2-Chloro-1,3-dimethylimidazolidinium chloride

2-Chloro-1,3-dimethylimidazolidinium chloride structure

2-Chloro-1,3-dimethylimidazolidinium chloride 

structure
  • CAS No:

    37091-73-9

  • Formula:

    C5H10ClN2.Cl

  • Chemical Name:

    2-Chloro-1,3-dimethylimidazolidinium chloride

  • Synonyms:

    DMC;1,3-DIMETHYL-2-CHLOROIMIDAZOLINIUM CHLORIDE;2-CHLORO-1,3-DIMETHYLIMIDAZOLIDINIUM CHLORIDE;2-CHLORO-1,3-DIMETHYLIMIDAZOLINIUM CHLORIDE;Chlorodimethyllimidazoliniumchloride;2-CHLORO-1,3-DIMETHYLIMIDAZOLINIUM CHLOR;2-CHLORO-1,3-DIMETHYLIMIDAZOLIUM CHLORIDE;2-CHLORO-1,3-DIMETHYLIMIDAZOLINIUM CHLORIDE: (CA. 25% IN DICHLOROMETHANE)

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

Brown Solid

2-Chloro-1,3-dimethylimidazolidinium chloride Basic Attributes

169.05

168.022110

1308068-626-2

56KA2A1U1D

2933290090

Characteristics

6.2

-2.93040

White to off-white Powder or Crystalline Powder

133-140 °C(lit.)

2-8°C

Safety Information

6.1

1593

3

36/37/38

26-36

Xi

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 41 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2-Chloro-1,3-dimethylimidazolidinium chloride Use and Manufacturing

Methods of Manufacturing

For 1000 ml three port in the reaction bottle, by adding 1, 3-dimethyl-2-imidazolidinone (34.2 g, 0.3 mol), carbon tetrachloride (400 ml), stirring slowly dropwise solid phosgene carbon tetrachloride solution (containing solid phosgene 30 g, 0.1 mole, carbon tetrachloride 100 ml), the reaction mixture is kept below 5 °C, violent mixing 0.5 hours, the reaction at room temperature 1 hour, heating to 50 °C, maintain 4 hours. To be the reaction product is cooled to room temperature, filter, a small amount of carbon tetrachloride washing, get a pure white crystalline product chloropivaloyl 1, 3-dimethyl-2-chlorotrifluoromethylbenzene imidazoline 49 g, yield of 96.6percent, Under an inert atmosphere, 1, 3-Dimethyl-2-imidazolidinone (7.0 mL, 64 mmol) was dissolved in anhydrous benzene (25 mL). To this oxalyl chloride (7.2 mL, 80 mmol) was added, and the solution was refluxed for 5 hours, and allowed to sit at room temperature overnight. The solution was filtered quickly to give 2-chloro-1, 3-dimethylimidazolinium chloride (7.5815 g, 44.85 mmol) in 70.1percent yield.1, 3-dimethyl-2-imidazolidinone 3.50g (30.7 mmol), and the mixture was heated for 5 hours and stirred at 140 of chloride phthalic acid 6.54g (32.4 mmol). After cooling, the crystal upon addition of 1, 4-dioxane 25mL precipitated, filtered with a glass filter, washed twice with 1, 4-dioxane 10 mL, washed once with ether 5 mL, and dried under vacuum. To give 2-chloro-1, 3-dimethyl imidazolium chloride 2.72g (53percent yield).

Uses

Used in the one-pot synthesis of 2-aminobenzimidazoles.

Computed Properties

Molecular Weight:169.05
Hydrogen Bond Acceptor Count:1
Exact Mass:168.0221037
Monoisotopic Mass:168.0221037
Topological Polar Surface Area:6.2
Heavy Atom Count:9
Complexity:115
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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