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179898-50-1

179898-50-1 Structure

179898-50-1 Structure
IdentificationBack Directory
[Name]

3-CHLORO-2-METHOXYPHENYLBORONIC ACID
[CAS]

179898-50-1
[Synonyms]

3-CHLORO-2-METHOXYPHENYLBORONIC ACID
3-Chloro-2-methoxybenzeneboronicacid
3-Chloro-2-methoxybenzeneboronic acid 99%
Boronic acid, B-(3-chloro-2-methoxyphenyl)-
Boronic acid, (3-chloro-2-methoxyphenyl)- (9CI)
[Molecular Formula]

C7H8BClO3
[MDL Number]

MFCD08277278
[MOL File]

179898-50-1.mol
[Molecular Weight]

186.4
Chemical PropertiesBack Directory
[Boiling point ]

356.9±52.0 °C(Predicted)
[density ]

1.32±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

solid
[pka]

7.58±0.58(Predicted)
[color ]

Off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
[HS Code ]

2931900090
Hazard InformationBack Directory
[Uses]

3-Chloro-2-methoxyphenylboronic Acid is a reagent used in the synthesis of a selective 17β-?HSD1 inhibitor in the therapeutic treatment of endometriosis.
[Synthesis]

1-Bromo-3-chloro-2-methoxybenzene

174913-10-1

Triisopropyl borate

5419-55-6

3-CHLORO-2-METHOXYPHENYLBORONIC ACID

179898-50-1

General procedure for the synthesis of 3-chloro-2-methoxyphenylboronic acid from 1-bromo-3-chloro-2-methoxybenzene and triisopropyl borate: 1-bromo-3-chloro-2-methoxybenzene (113.2 g, 426.4 mmol) was dissolved in tetrahydrofuran (1000 mL), and cooled to -78°C. At the same temperature 1.7 M tertiary-butyllithium (t-BuLi) was added slowly to a tert-butyl lithium (t-BuLi) ) to a hexane solution (251.7 mL, 426.4 mmol). The reaction mixture was stirred at -78°C for 1 h. Triisopropyl borate (B(OiPr)3) (113.2 mL, 852.4 mmol) was added, followed by gradual warming of the reaction mixture to room temperature and continued stirring for 3 hours. Upon completion of the reaction, 2 N aqueous hydrochloric acid (800 mL) was added to the mixture and stirred at room temperature for 1.5 hours. The resulting precipitate was collected by filtration, washed sequentially with water and ether and dried under vacuum. The crude product was recrystallized by a solvent mixture of chloroform and ethyl acetate and dried to give 3-chloro-2-methoxyphenylboronic acid as a white solid (89.6 g, 91% yield; Mass Spectrometry (MS): [M + H]+ = 230.

[References]

[1] Patent: KR2018/10165, 2018, A. Location in patent: Paragraph 0207-0210
Spectrum DetailBack Directory
[Spectrum Detail]

3-CHLORO-2-METHOXYPHENYLBORONIC ACID(179898-50-1)1HNMR
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