(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol

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(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol Basic information
Product Name:(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol
Synonyms:(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol;3-Fluoro-4-(hydroxymethyl)phenylboronic acid Pinacol Ester;2-fluoro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanol;Benzenemethanol, 2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-;2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan.
CAS:1082066-29-2
MF:C13H18BFO3
MW:252.09
EINECS:
Product Categories:
Mol File:1082066-29-2.mol
(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol Structure
(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol Chemical Properties
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
AppearanceWhite to off-white Solid
Safety Information
HS Code 2934999090
MSDS Information
(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol Usage And Synthesis
Synthesis
Bis(pinacolato)diboron

73183-34-3

4-BROMO-2-FLUOROBENZYL ALCOHOL

188582-62-9

(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol

1082066-29-2

3.1.1. Preparation of (2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol (934-2) To a stirred solution of 4-bromo-2-fluorobenzyl alcohol (500 mg, 2.44 mmol) in dioxane (5 mL) under nitrogen protection was sequentially added pinacol ester of biboronate (929 mg, 3.66 mmol), [1,1'-bis(diphenylphosphino)ferrocene]palladium dichloride dichloromethane complex (198 mg, 0.24 mmol) and potassium acetate (717 mg, 7.32 mmol). The reaction mixture was stirred at 90 °C overnight. After completion of the reaction, the mixture was cooled to room temperature and extracted with ethyl acetate and water by partitioning. The organic layer was separated, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure and the resulting crude product was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate, 0-20% gradient) to afford the title compound (2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol (934-2) (300 mg, 48% yield) as a yellow oil.

References[1] Patent: US2018/194762, 2018, A1. Location in patent: Paragraph 0740-0741
[2] Bioorganic and Medicinal Chemistry, 2018, vol. 26, # 18, p. 4984 - 4995
(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol Preparation Products And Raw materials
Raw materialsBis(pinacolato)diboron-->4-Bromo-2-fluorobenzyl alcohol-->1,4-Dioxane-->Potassium Acetate
Tag:(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol(1082066-29-2) Related Product Information
3-fluoro-4-(hydroxyMethyl)phenylboronic acid Methyl 2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde 4-CarBoxy-3-fluoroBenzeneBoronicacid,pinacolester Benzenemethanol, 2,5-difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- 2-[3-Fluoro-4- (methoxymethyl)phenyl]-4,4,5,5- tetramethyl-1,3,2-dioxaborolane