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943994-02-3

943994-02-3 Structure

943994-02-3 Structure
IdentificationBack Directory
[Name]

6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-benzo[b][1,4]oxazin-3(4H)-one
[CAS]

943994-02-3
[Synonyms]

-2H-benzo[b][1,4]oxazin-3(4H)
3-Oxo-2H,4H-benzo[b][1,4]oxazine-6-boronic acid pinacol ester
6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4H-1,4-benzo...
3-Oxo-3,4-dihydro-2H-1,4-benzoxazine-6-boronic acid pinacol ester
3-Oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-6-boronic Acid Pinacol Ester
6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-4H-1,4-benzoxazin-3-one
6-(4,4,5,5-tetraMethyl-1-3,2-dioxaborolan-2-yl)-2H-1,4-benzoxazin-3(4H)-one
2H-1,4-Benzoxazin-3(4H)-one,6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-
6-(tetraMethyl-1,3,2-dioxaborolan-2-yl)-3,4- dihydro-2H-1,4-benzoxazin-3-one
6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-benzo[b][1,4]oxazin-3(4H)-one
3-hydroxy-2,3-dimethylbutan-2-yl hydrogen (3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)boronate
[Molecular Formula]

C14H18BNO4
[MDL Number]

MFCD12755796
[MOL File]

943994-02-3.mol
[Molecular Weight]

275.11
Chemical PropertiesBack Directory
[Boiling point ]

441.1±45.0 °C(Predicted)
[density ]

1.20±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[form ]

Solid
[pka]

12.75±0.20(Predicted)
[Appearance]

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

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H315-H319
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Spectrum DetailBack Directory
[Spectrum Detail]

6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-benzo[b][1,4]oxazin-3(4H)-one(943994-02-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-BROMO-2H-1,4-BENZOXAZIN-3(4H)-ONE

24036-52-0

Bis(pinacolato)diboron

73183-34-3

6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-benzo[b][1,4]oxazin-3(4H)-one

943994-02-3

6-Bromo-2H-1,4-benzoxazin-3(4H)-one (2.3 g, 10 mmol) and pinacol ester of bis(boronic acid) (3.05 g, 12 mmol) were used as raw materials, which were dissolved in dioxane (20 mL), and then potassium acetate (2 g, 20 mmol) and Pd(dppf)Cl2 (730 mg, 1 mmol) were added sequentially. The reaction system was purged with nitrogen and the reaction was stirred at 90 °C overnight. After completion of the reaction, the mixture was diluted with ethyl acetate (200 mL) and filtered. The organic phase was sequentially washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain the crude product. The crude product was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate=3:1) to afford 3-oxo-2H,4H-benzo[b][1,4]oxazine-6-boronic acid pinacol ester (1.9 g, 69% yield).

[References]

[1] Patent: WO2015/153683, 2015, A1. Location in patent: Paragraph 0937
[2] Patent: WO2017/211303, 2017, A1. Location in patent: Page/Page column 36
[3] Patent: WO2010/116282, 2010, A1. Location in patent: Page/Page column 55-56
[4] Patent: WO2007/77961, 2007, A2. Location in patent: Page/Page column 227
[5] Patent: KR2016/37198, 2016, A. Location in patent: Paragraph 3281-3283
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