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ChemicalBook >  Product Catalog >  Organic Chemistry >  Hydrocarbons and derivatives >  Hydrocarbon halides >  1,1-DIBROMO-2,2-BIS(CHLOROMETHYL)CYCLOPROPANE

1,1-DIBROMO-2,2-BIS(CHLOROMETHYL)CYCLOPROPANE

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1,1-DIBROMO-2,2-BIS(CHLOROMETHYL)CYCLOPROPANE Basic information

Product Name:
1,1-DIBROMO-2,2-BIS(CHLOROMETHYL)CYCLOPROPANE
Synonyms:
  • Cyclopropane,1,1-dibroMo-2,2-bis(chloroMethyl)-
  • 1,1-DibroMo-2,2-bis(chloroMethyl)cyclopropane 90%, technical grade
  • 1,1-DIBROMO-2,2-BIS(CHLOROMETHYL)CYCLOPROPANE
  • 1,1-BIS(CHLOROMETHYL)-2,2-DIBROMOCYCLOPROPANE
  • AKOS BBS-00001998
  • 1,1-DIBROMO-2,2-BIS(CHLOROMETHYL)-CYCLOP ROPANE, TECH., 90%
  • 2,2-Bis-(chloromethyl)-1,1-dibromocyclopropane
  • EOS-60772
CAS:
98577-44-7
MF:
C5H6Br2Cl2
MW:
296.82
EINECS:
627-508-0
Product Categories:
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • Alkyl
Mol File:
98577-44-7.mol
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1,1-DIBROMO-2,2-BIS(CHLOROMETHYL)CYCLOPROPANE Chemical Properties

Melting point:
48-50 °C (lit.)
Boiling point:
277.1±10.0 °C(Predicted)
Density 
2.065±0.06 g/cm3 (20 ºC 760 Torr)
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
color 
White to Orange to Green
InChI
InChI=1S/C5H6Br2Cl2/c6-5(7)1-4(5,2-8)3-9/h1-3H2
InChIKey
RCRVZCIUKQNOIS-UHFFFAOYSA-N
SMILES
C1(Br)(Br)CC1(CCl)CCl
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2902190000

MSDS

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1,1-DIBROMO-2,2-BIS(CHLOROMETHYL)CYCLOPROPANE Usage And Synthesis

Uses

1,1-Dibromo-2,2-bis(chloromethyl)cyclopropane may be used as a starting material in the synthesis of [1.1.1]-propellane and ((3-ethynylbicyclo[1.1.1]pentan-1-yl)ethynyl)trimethylsilane.

Preparation

1000 ml 1,1-bis(chloromethyl)-2,2-dibromocyclopropane was added  to a vigorously stirred mixture within 10-15 min, which contains bromoform (370 ml, 4.24 mol), 3-chloro-2-chloromethyl-1-propane (250 g, 2.0 mol), 10 g benzyltriethylammonium chloride, 8 ml ethanol and 200 ml methylene chloride . The temperature was maintained between 25°-35° C. After overnight stirring, 500 ml methylene chloride was added and the thick black mixture was allowed to separate into layers. The top aqueous layer was removed and the bottom layer was gently washed with water (500 ml). 500 ml water was then added and well shaken. Separated the organic phase, treated the residual emulsion with solid sodium chloride and filtered through Celite. All aqueous layers were washed with methylene chloride. The organic extracts were combined, dried over magnesium sulfate, and filtered through Celite. Concentration and vacuum distillation gave the mixture of starting material and black-brown residue which was distilled on a Kugel-Rohr giving  semicrystalline fraction containing the product. Crystallization from 400 ml of pentane from a dry ice-acetone bath gave the white wet crystals. The crude product was dissolved in 400 ml of penfane, then 7.5 g silica gel was added.  Filtered and low temperature recrystallized again. Finally, obtain the product (1,1-DIBROMO-2,2-BIS(CHLOROMETHYL)CYCLOPROPANE )

General Description

1,1-Dibromo-2,2-bis(chloromethyl)cyclopropane is a halogenated cyclopropane derivative. It has been reported to be synthesized from 3-chloro-2-(chloromethyl)-1-propene. It is formed as an intermediate during the synthesis of [1.1.1]propellane by Szeimies method.

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