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121554-18-5

121554-18-5 Structure

121554-18-5 Structure
IdentificationBack Directory
[Name]

(4'-Pentyl[1,1'-biphenyl]-4-yl)-boronic acid
[CAS]

121554-18-5
[Synonyms]

-pentyl[1,1'
(4'-Pentyl-[1,1'-biphenyl]-4-yl)
4-(4-pentylphenyl)phenyl]boronicaci
[4-(4-pentylphenyl)phenyl]boronic Acid
(4'-Pentyl[1,1'-biphenyl]-4-yl)-boronic acid
Boronic acid, (4'-pentyl[1,1'-biphenyl]-4-yl)-
Boronic acid, B-(4'-pentyl[1,1'-biphenyl]-4-yl)-
4'-Pentyl-4-biphenylboronic Acid (contains varying amounts of Anhydride)
[Molecular Formula]

C17H21BO2
[MDL Number]

MFCD07644474
[MOL File]

121554-18-5.mol
[Molecular Weight]

268.158
Chemical PropertiesBack Directory
[Boiling point ]

436.4±48.0 °C(Predicted)
[density ]

1.08±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

8.61±0.17(Predicted)
[color ]

White to Almost white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2931900090
Hazard InformationBack Directory
[Chemical Properties]

off-white powder
[Synthesis]

4-BROMO-4'-N-PENTYLBIPHENYL

63619-59-0

(4'-Pentyl[1,1'-biphenyl]-4-yl)-boronic acid

121554-18-5

General procedure for the synthesis of 4-pentylbiphenylboronic acid from 4'-bromo-4-pentylbiphenyl: 4'-bromo-4-pentylbiphenyl (3 g, 9.9 mmol) was added in a single addition to magnesium shavings (0.27 g, 11.1 mmol) in an iodine-catalyzed reaction using tetrahydrofuran (40 mL) as solvent. The reaction mixture was heated at reflux for 3 h and subsequently cooled to -78 °C and trimethyl borate (2.06 g, 19.8 mmol) was added slowly and dropwise. The reaction system was gradually warmed to room temperature over 1 h, then acidified with 2 M hydrochloric acid (50 mL) and extracted with ether (3 x 50 mL). The combined ether extracts were back-extracted with 1 M sodium hydroxide solution (100 mL). The aqueous phase was acidified with concentrated hydrochloric acid and extracted again with ether (3×50 mL), the organic phase was dried with anhydrous magnesium sulfate, and the solvent was removed by concentration under reduced pressure to obtain 4-pentylbiphenylboronic acid (2.07 g, 78% yield), the product was an off-white powder.

[References]

[1] Patent: EP2098520, 2009, A1. Location in patent: Page/Page column 18
[2] Tetrahedron Letters, 2014, vol. 55, # 9, p. 1631 - 1634
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