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478375-39-2

478375-39-2 Structure

478375-39-2 Structure
IdentificationBack Directory
[Name]

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

478375-39-2
[Synonyms]

3-(Methoxycarbonyl)-4-methylphenylboronic acid, pinacol ester
Methyl 2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)
Methyl 2-Methyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzoate
Benzoic acid, 2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, methyl ester
[Molecular Formula]

C15H21BO4
[MDL Number]

MFCD16996355
[MOL File]

478375-39-2.mol
[Molecular Weight]

276.14
Chemical PropertiesBack Directory
[Boiling point ]

370.4±35.0 °C(Predicted)
[density ]

1.07±0.1 g/cm3(Predicted)
[storage temp. ]

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

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

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2931900090
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 2-Methyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzoate(478375-39-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

BENZOIC ACID, 5-IODO-2-METHYL-, METHYL ESTER

103440-54-6

Bis(pinacolato)diboron

73183-34-3

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

478375-39-2

General procedure for the synthesis of 3-(methoxycarbonyl)-4-methylphenylboronic acid pinacol ester from methyl 5-iodo-2-methylbenzoate and pinacol ester of bisboronic acid: methyl 5-iodo-2-methylbenzoate (0.25 mol), pinacol ester of bisboronic acid (100 g, 0.40 mol) and potassium acetate (92 g, 0.93 mol) were added to DMF (800 mL) , which was subsequently degassed with nitrogen. [1,1'-Bis(diphenylphosphino)ferrocene]palladium(II) dichloride complex with dichloromethane (6 g) was added and the reaction mixture was heated to 100 °C and kept for 18 hours. After completion of the reaction, it was cooled to room temperature, filtered through diatomaceous earth and washed with ethyl acetate (3 x 1 L). The filtrates were combined, washed with brine (3 x 500 mL), dried over anhydrous sodium sulfate and concentrated in vacuum. The residue was washed with petroleum ether (2 × 500 mL), filtered and dried to afford 3-(methoxycarbonyl)-4-methylphenylboronic acid pinacol ester as a yellow powder (60 g, 87% yield), which was used directly in the next reaction.

[References]

[1] Patent: WO2015/189744, 2015, A1. Location in patent: Page/Page column 72
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