ChemicalBook--->CAS DataBase List--->642494-37-9

642494-37-9

642494-37-9 Structure

642494-37-9 Structure
IdentificationBack Directory
[Name]

Indole-7-boronic acid pinacol ester
[CAS]

642494-37-9
[Synonyms]

INDOLE-7-BORONIC ACID PINACOL ESTER
1H-INDOL-7-YLBORONIC ACID PINACOL ESTER
1H-Indole-7-boronic acid, pinacol ester
REF DUPL: Indole-7-boronic acid pinacol ester
7-(tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
7-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-INDOLE
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3H-indole
1H-Indole, 7-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-
3-hydroxy-2,3-dimethylbutan-2-yl hydrogen 1H-indol-7-ylboronate
7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole, 2-(1H-Indol-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
[Molecular Formula]

C14H18BNO2
[MDL Number]

MFCD08669591
[MOL File]

642494-37-9.mol
[Molecular Weight]

243.11
Chemical PropertiesBack Directory
[Melting point ]

94-96 °C
[Boiling point ]

396.0±15.0 °C(Predicted)
[density ]

1.11±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

crystalline powder
[pka]

17.01±0.30(Predicted)
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P280-P271
[Hazard Codes ]

Xi
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

Indole-7-boronic acid, pinacol ester
[Synthesis]

7-Bromoindole

51417-51-7

Bis(pinacolato)diboron

73183-34-3

Indole-7-boronic acid pinacol ester

642494-37-9

The general procedure for the synthesis of 7-bromoindole and pinacol ester of bis(pinacolato) borate from 7-bromoindole and pinacol ester of bis(pinacolato) borate was as follows: 7-bromoindole (20 g, 0.102 mol) was dissolved in a 1 L single-necked flask containing DMSO (100 mL), and bis(pinacolato)diboron (39 g, 0.153 mol), [1,1'-bis(diphenylphosphinato)ferrocene]dichloro palladium (Pd(dppf)Cl2, 4 g, 0.005 mol) and potassium acetate (15 g, 0.153 mol). The reaction system was heated to 85 °C and the reaction was stirred for 2 hours. After completion of the reaction, the reaction was quenched by the addition of water. The mixture was extracted three times with ethyl acetate, the organic phases were combined and dried over anhydrous sodium sulfate. After concentration under reduced pressure, the product was purified by column chromatography to afford the target product 7-indoleboronic acid pinacol ester (25 g, 0.103 mol). The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3) and mass spectrometry (ESI): 1H NMR (400 MHz, CDCl3) δ 9.29 (s, 1H), 7.82 (d, J = 7.9 Hz, 1H), 7.70 (d, J = 7.0 Hz, 1H), 7.32-7.29 (m, 1H), 7.21- 7.14 (m, 1H), 6.62-6.57 (m, 1H), 1.44 (s, 12H); MS (ESI) m/z: [M + H]+ 244.1.

[References]

[1] Synlett, 2003, # 8, p. 1204 - 1206
[2] Advanced Synthesis and Catalysis, 2017, vol. 359, # 19, p. 3421 - 3427
[3] Journal of the American Chemical Society, 2017, vol. 139, # 24, p. 8267 - 8276
[4] European Journal of Organic Chemistry, 2016, vol. 2016, # 27, p. 4621 - 4628
[5] Patent: JP2015/528445, 2015, A. Location in patent: Paragraph 0047; 0065
Spectrum DetailBack Directory
[Spectrum Detail]

Indole-7-boronic acid pinacol ester(642494-37-9)1HNMR
Indole-7-boronic acid pinacol ester(642494-37-9)FT-IR
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