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1,3-Dibromoadamantane

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1,3-Dibromoadamantane Basic information

Product Name:
1,3-Dibromoadamantane
Synonyms:
  • 1,3-DIBROMOADAMANTANE
  • 1,3-DIBROMOTRICYCLO[3.3.1.1(3,7)]DECANE
  • 1,3-DIBROMO- ADAMANTINE
  • Dibromoadamantane,97%
  • tricyclo[3.3.1.1~3,7~]decane, 1,3-dibromo-
  • 1,3-Dibromoadamantan
  • Adamantane, 1,3-dibromo-
  • NSC 102289
CAS:
876-53-9
MF:
C10H14Br2
MW:
294.03
EINECS:
1533716-785-6
Product Categories:
  • Alkyl
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • Adamantane derivatives
  • Miscellaneous Reagents
  • Adamantanes
Mol File:
876-53-9.mol
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1,3-Dibromoadamantane Chemical Properties

Melting point:
108-110 °C (lit.)
Boiling point:
287.6±13.0 °C(Predicted)
Density 
1.864±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly)
form 
Solid
color 
White to Pale Gray
InChI
InChI=1S/C10H14Br2/c11-9-2-7-1-8(4-9)5-10(12,3-7)6-9/h7-8H,1-6H2
InChIKey
HLWZKLMEOVIWRK-UHFFFAOYSA-N
SMILES
C12(Br)CC3CC(CC(Br)(C3)C1)C2
CAS DataBase Reference
876-53-9(CAS DataBase Reference)
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Safety Information

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

MSDS

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1,3-Dibromoadamantane Usage And Synthesis

Chemical Properties

White Solid

Uses

1,3-Dibromoadamantane may be used in the preparation of 1,3-bis(phenyldimethylsilyl)adamantine.

General Description

1,3-Dibromoadamantane is reported to react with diphenylphosphide ions (Ph2P-) under photostimulation by the SRN1 mechanism. The viscosity-dependent retarding effect of 1,3-dibromoadamantane in highly viscous polymeric chlorotrifluoroethene has been studied by 13C NMR relaxation measurements. Preparation of 1,3-dibromoadamantane via dibromination of adamantine has been reported.

Synthesis

281-23-2

768-90-1

876-53-9

Reactions were carried out in 20 mL glass ampoules or 17 mL stainless steel pressure microreactors with consistent results from parallel experiments. Under argon protection, 0.3 mmol of tris(acetylacetonato)iron(III) [Fe(acac)3], 10 mmol of adamantane, 10 mmol of carbon tetrabromide (CBr4), and 150 mmol of dibromomethane (CH2Br2) were added to the microreactor (or ampoule). The reactor (or ampoule) was sealed and heated under stirring conditions. After completion of the reaction, the reactor (or ampoule) was cooled to room temperature, opened and the solvent was removed by distillation and the residue was purified by crystallization with hexane or ethanol. The conversion of adamantane and the yield of its derivatives were determined by gas chromatography (GLC) using decene as an internal standard with correction factors of 1.09 and 1.53 for adamantane and bromoadamantane, respectively.The structures of the resulting compounds were confirmed by comparison with known samples and literature data.

References

[1] Russian Journal of Organic Chemistry, 2015, vol. 51, # 2, p. 184 - 187
[2] Zh. Org. Khim., 2015, vol. 51, # 2, p. 196 - 199
[3] Tetrahedron Letters, 1986, vol. 27, # 12, p. 1399 - 1402
[4] Journal of Organic Chemistry USSR (English Translation), 1984, vol. 20, p. 2041
[5] Zhurnal Organicheskoi Khimii, 1984, vol. 20, # 10, p. 2239 - 2240

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