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ChemicalBook--->CAS DataBase List--->312303-48-3

312303-48-3

312303-48-3 Structure

312303-48-3 Structure
IdentificationBack Directory
[Name]

2-Methylnaphthalene-1-boronic Acid Pinacol Ester
[CAS]

312303-48-3
[Synonyms]

2-Methylnaphthalene-1-boronic Acid Pinacol Ester
4,4,5,5-tetramethyl-2-(2-methylnaphthalen-1-yl)-1,3,2-dioxaborolane
4,4,5,5-tetramethyl-2-(2-methyl-1-naphthalenyl)-1,3,2-Dioxaborolane
1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-methyl-1-naphthalenyl)-
[Molecular Formula]

C17H21BO2
[MDL Number]

MFCD22189526
[MOL File]

312303-48-3.mol
[Molecular Weight]

268.16
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[Appearance]

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


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

2-Methylnaphthalene-1-boronic Acid Pinacol Ester(312303-48-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

61676-62-8

1-BROMO-2-METHYLNAPHTHALENE

2586-62-1

2-Methylnaphthalene-1-boronic Acid Pinacol Ester

312303-48-3

The general procedure for the synthesis of 4,4,5,5-tetramethyl-2-(2-methylnaphthalen-1-yl)-1,3,2-dioxaborolanes from isopropanol pinacol borate and 1-bromo-2-methylnaphthalene was as follows: 1,2-dibromoethane (ca. 0.3 ml) was added dropwise to 1000 cm3 THF solution containing 6.10 g (0.25 mol) of magnesium chips. The mixture was stirred for 10 minutes and then continued to stir vigorously for 3.5 hours at room temperature. Subsequently, 55.3 g (0.25 mol) of 1-bromo-2-methylnaphthalene was added and 46.5 g (250 mmol) of 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborole was added all at once. The reaction mixture was stirred for 15 minutes and then the reaction was terminated by pouring into 1000 cm3 cold water. The product was extracted with 3 x 300 ml of ethyl acetate, the organic layers were combined, washed sequentially with water and brine, and dried over anhydrous MgSO? The solvent was removed by evaporation under reduced pressure to give a white solid. The solid was washed with 2×75 ml pentane and dried in vacuum to give the product 47.3 g in 70% yield. Elemental analysis (C17H21BO2) Calculated value: C, 76.14; H, 7.89. Measured value: C, 76.21; H, 7.96.1H NMR (CDCl?) δ: 8.12 (m, 1H, 8-H), 7.77 (m, 1H, 5-H), 7.75 (d, J=8.4 Hz, 1H, 4-H), 7.44 (m, 1H. 7-H), 7.38 (m, 1H, 6-H), 7.28 (d, J=8.4Hz, 1H, 3-H), 2.63 (s, 3H, 2-Me), 1.48 (s, 12H, CMe?CMe?).

[References]

[1] Patent: WO2015/134213, 2015, A1. Location in patent: Page/Page column 42; 43
[2] Patent: WO2018/5201, 2018, A1. Location in patent: Page/Page column 27
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