Basic information Safety Supplier Related

Boronic acid, (5-cyano-2-methoxyphenyl)- (9CI)

Basic information Safety Supplier Related

Boronic acid, (5-cyano-2-methoxyphenyl)- (9CI) Basic information

Product Name:
Boronic acid, (5-cyano-2-methoxyphenyl)- (9CI)
Synonyms:
  • Boronic acid, (5-cyano-2-methoxyphenyl)- (9CI)
  • 5-Cyano-2-Methoxyphenylboronic acid, >95%
  • Boronic acid, B-(5-cyano-2-methoxyphenyl)-
CAS:
612833-37-1
MF:
C8H8BNO3
MW:
176.96
Product Categories:
  • METHOXY
Mol File:
612833-37-1.mol
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Boronic acid, (5-cyano-2-methoxyphenyl)- (9CI) Chemical Properties

Melting point:
211-212°
Boiling point:
412.4±55.0 °C(Predicted)
Density 
1.26±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,2-8°C
pka
7.19±0.58(Predicted)
Appearance
Off-white to light yellow Solid
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Safety Information

HazardClass 
IRRITANT
HS Code 
2931900090
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Boronic acid, (5-cyano-2-methoxyphenyl)- (9CI) Usage And Synthesis

Synthesis

5419-55-6

117572-79-9

612833-37-1

The general procedure for the synthesis of 2-methoxy-5-cyanophenylboronic acid from triisopropyl borate and 3-bromo-4-methoxybenzonitrile was as follows: firstly, 3-bromo-4-methoxybenzonitrile (7.7 g, 36 mmol) and triisopropyl borate (14 g, 73 mmol) were dissolved in tetrahydrofuran (150 mL), and then at -78 °C, 2.5 mol/L of n butyl lithium (hexane solution, 22 mL, 55 mmol), and the addition process lasted for 20 min. After the reaction mixture was stirred at -78 °C for 2 h, 7% phosphoric acid (100 mL) was added and the mixture was gradually warmed to room temperature. Subsequently, the reaction mixture was partitioned by adding dichloromethane to the organic layer and extracting the mixture with 5% aqueous sodium hydroxide (200 mL). The aqueous layer was washed with ether and adjusted to pH 2.5 with 85% phosphoric acid and the insoluble material was collected by filtration. The resulting solid was washed with water and dried to give the final 2-methoxy-5-cyanophenylboronic acid (5.1 g, 29 mmol, 79% yield). The product was detected by mass spectrometry (ESI) at m/z 178 (M+H)+; 1H NMR (300 MHz, DMSO-d6) δ 8.03 (s, 2H), 7.86-7.78 (m, 2H), 7.13 (d, J=11.6 Hz, 1H), 3.85 (s, 3H).

References

[1] Patent: US2016/332999, 2016, A1. Location in patent: Paragraph 0649; 0650; 0651
[2] Patent: EP3330266, 2018, A1. Location in patent: Paragraph 0169

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