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590418-05-6

590418-05-6 Structure

590418-05-6 Structure
IdentificationBack Directory
[Name]

2-Methyl-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)aniline
[CAS]

590418-05-6
[Synonyms]

4-Amino-3-methylphenylboronic acid, pinacol ester
2-Methyl-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)aniline
2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenamine
Benzenamine, 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
[Molecular Formula]

C13H20BNO2
[MOL File]

590418-05-6.mol
[Molecular Weight]

233.11
Chemical PropertiesBack Directory
[Boiling point ]

359.0±35.0 °C(Predicted)
[density ]

1.03±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

4.09±0.10(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

2-Methyl-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)aniline(590418-05-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-BROMO-2-METHYLANILINE

583-75-5

Bis(pinacolato)diboron

73183-34-3

2-Methyl-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)aniline

590418-05-6

General procedure for the synthesis of 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline from 2-methyl-4-bromoaniline and pinacol bis(boronic acid) ester: To a solution of 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (1.05 g, 0.134 mmol) containing 4-bromo-2-methylaniline (500 mg, 2.69 mmol), potassium acetate (1.32 g, 13.4 mmol) and bis(pinacolato)diboron ( 2.05 g, 8.0 mmol) to a solution of dioxane (4 mL) was added Pd(dppf)Cl2 (110 mg, 0.134 mmol). After degassing and replacement with nitrogen, the reaction mixture was refluxed for 16 h at 85 °C. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, water (20 mL) was added and the mixture was extracted with ethyl acetate (30 mL x 3). The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated, and finally purified by silica gel column chromatography (eluent: dichloromethane) to afford the target compound 13-2 as a white solid (485 mg, 77% yield).

[References]

[1] Patent: US9138427, 2015, B2. Location in patent: Page/Page column 291
[2] Patent: WO2012/104305, 2012, A1. Location in patent: Page/Page column 150
[3] Patent: EP3034078, 2016, A1. Location in patent: Paragraph 0241-0242
[4] Patent: US2005/171131, 2005, A1. Location in patent: Page/Page column 54-55
[5] Patent: US2006/25383, 2006, A1. Location in patent: Page/Page column 54
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