Identification | Back Directory | [Name]
[4'-(pentyloxy)[1,1'-biphenyl]-4-yl]boronic acid | [CAS]
158937-25-8 | [Synonyms]
4-pentoxyl biphenyl boric acid 4'-Amyloxybiphenyl-4-boronic Acid 4'-Pentyloxybiphenyl-4-boronic Acid 4'-Pentyloxyl-4-biphenylboronic aci 4'-Pentyloxyl-4-biphenylboronic acid 4'-(Pentyloxy)biphenyl-4-ylboronic acid 4-(4-n-pentyloxyphenyl)phenylboronic acid 4'-n-Pentyloxybiphenyl-4-boronic acid, 97% 4-'(Penthloxy)[1,1’-biphenyl-4-yl]-boronic acid (4'-(Pentyloxy)-[1,1'-biphenyl]-4-yl)boronicaci [4'-(pentyloxy)[1,1'-biphenyl]-4-yl]boronic acid [4'-(Pentyloxy)[1,1'-biphenyl]-4-yl]- Boronic acidc Boronic acid, B-[4'-(pentyloxy)[1,1'-biphenyl]-4-yl]- [4'-(Pentyloxy)[1,1'-biphenyl]-4-yl]boronic acid 4'-Pentyloxybiphenyl-4-boronic Acid (contains varying amounts of Anhydride) | [Molecular Formula]
C17H21BO3 | [MDL Number]
MFCD07644475 | [MOL File]
158937-25-8.mol | [Molecular Weight]
284.158 |
Chemical Properties | Back Directory | [Melting point ]
197°C(lit.) | [Boiling point ]
459.9±55.0 °C(Predicted) | [density ]
1.11 | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [form ]
powder to crystal | [pka]
8.63±0.17(Predicted) | [color ]
White to Almost white | [CAS DataBase Reference]
158937-25-8 |
Hazard Information | Back Directory | [Synthesis]
General method: n-Butyl lithium (n-BuLi, 2.5 M, 7.4 mL, 18 mmol) was slowly added dropwise to a solution of methyl tertiary butyl ether (MTBE, 50 mL) of 4-bromo-4'-(pentyloxy)biphenyl (4.5 g, 13 mmol) at -20 °C under nitrogen protection. After stirring the reaction mixture for 2 h, it was cooled to -60 °C and tetrahydrofuran (THF, 6 mL) was added. Subsequently, a solution of triisopropoxyborane ((i-PrO)3B, 6.1 mL, 26 mmol) in methyl tert-butyl ether (MTBE, 8 mL) was slowly added dropwise to the reaction mixture and stirring was continued for 1 hour. The reaction mixture was gradually warmed to room temperature and stirred overnight. The reaction mixture was treated with 2M hydrochloric acid (HCl, 50 mL) for 10 minutes. The organic layer was separated and concentrated under reduced pressure to remove the solvent. Hexane (40 mL) was added to the residue and stirred for 10 minutes. After filtration, the filter cake was washed with a solvent mixture of hexane-methyl tert-butyl ether (8:1) to afford (4'-(pentyloxy)-[1,1'-biphenyl]-4-yl)boronic acid (15c, 3.7 g, 91.4% yield) as a white solid. | [References]
[1] European Journal of Medicinal Chemistry, 2012, vol. 50, p. 196 - 208 [2] Molecular Crystals and Liquid Crystals Science and Technology Section A: Molecular Crystals and Liquid Crystals, 2000, vol. 339, p. 145 - 158 |
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