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ACENAPHTHENE-5-BORONIC ACID

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ACENAPHTHENE-5-BORONIC ACID Basic information

Product Name:
ACENAPHTHENE-5-BORONIC ACID
Synonyms:
  • Acenaphthelene-5-boronicacid
  • BB-8189Acenaphthene-5-boronic acid
  • (1,2-dihydroacenaphthylen-5-yl)boronic acid
  • Boronic acid, B-(1,2-dihydro-5-acenaphthylenyl)-
  • Acenaphthene-5-boronicaci
  • (1,2-Dihydroacenaphthylen-5-yl)boronic acid - [D88418]
CAS:
183158-33-0
MF:
C12H11BO2
MW:
198.03
Product Categories:
  • Aryl
  • Boronic Acids
  • Boronic Acids and Derivatives
  • blocks
  • BoronicAcids
Mol File:
183158-33-0.mol
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ACENAPHTHENE-5-BORONIC ACID Chemical Properties

Melting point:
270 °C(lit.)
Boiling point:
429.9±53.0 °C(Predicted)
Density 
1.28±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
9.11±0.20(Predicted)
Appearance
White to off-white Solid
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Safety Information

WGK Germany 
3
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ACENAPHTHENE-5-BORONIC ACID Usage And Synthesis

Application

Naphthalene-5-boronic acid can be used as a pharmaceutical synthesis intermediate and can be used in laboratory organic synthesis processes and chemical and pharmaceutical synthesis processes.

Synthesis

Acenaphthene-5-boronic acid was prepared as follows: 11.7 g of commercial 5-bromoacenaphthene was dissolved in a solvent mixture of 50 ml of anhydrous toluene and 50 ml of anhydrous ether, and the resulting solution was cooled under argon atmosphere to -40??C. 35 ml of a 1.6 M n-butyllithium solution in hexanes was added dropwise to the resulting solution, and the temperature was subsequently raised to -10??C. After 2 hours, the resulting solution was cooled to -70??C. Another solution made by dissolving 35 ml of triisopropoxyborane in 50 ml of ether was added dropwise to this solution. The resulting solution was stirred at -70??C for 3 hours and then left overnight. After overnight, the resulting solution was acidified with 10% by weight of dilute hydrochloric acid and the organic layer was extracted with toluene. The organic layer was washed with dilute hydrochloric acid and saturated sodium chloride solution, dried over anhydrous sodium sulfate, and the organic solvent was distilled using an evaporator. The residue was crystallized using toluene/hexane to give 4.5 g (45% yield) of acenaphthene-5-boronic acid.

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