ACENAPHTHENE-5-BORONIC ACID
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
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
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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