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2-Ethoxycarbonylphenylboronic acid pinacol ester

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2-Ethoxycarbonylphenylboronic acid pinacol ester Basic information
Product Name:2-Ethoxycarbonylphenylboronic acid pinacol ester
Synonyms:2-ETHOXYCARBONYLPHENYLBORONIC ACID, PINACOL ESTER;ETHYL 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOATE;Ethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate,min.97%;2-carboethoxyphenylboronic acid pinacol ester;Ethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate, min. 97%;2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(ethoxycarbonyl)benzene;2-(Ethoxycarbonyl)phenylboronic acid, pinacol cyclic ester;2-Carboethoxyphenylboronic acid pinacol ester, Ethyl 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
CAS:269409-99-6
MF:C15H21BO4
MW:276.14
EINECS:
Product Categories:Heterocyclic Compounds;organic or inorganic borate
Mol File:269409-99-6.mol
2-Ethoxycarbonylphenylboronic acid pinacol ester Structure
2-Ethoxycarbonylphenylboronic acid pinacol ester Chemical Properties
Melting point 60-65 °C
Boiling point 378.0±25.0 °C(Predicted)
density 1.07±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Powder
color white to yellow
InChI1S/C15H21BO4/c1-6-18-13(17)11-9-7-8-10-12(11)16-19-14(2,3)15(4,5)20-16/h7-10H,6H2,1-5H3
InChIKeyRFBZWPFBCXBBJS-UHFFFAOYSA-N
SMILESCCOC(=O)c1ccccc1B2OC(C)(C)C(C)(C)O2
CAS DataBase Reference269409-99-6(CAS DataBase Reference)
Safety Information
Safety Statements 24/25
WGK Germany 3
HS Code 2931900090
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
2-Ethoxycarbonylphenylboronic acid pinacol ester Usage And Synthesis
Synthesis
Ethyl 2-Chlorobenzoate

7335-25-3

Bis(pinacolato)diboron

73183-34-3

2-Ethoxycarbonylphenylboronic acid pinacol ester

269409-99-6

Under argon protection, 7.0 mg (0.025 mmol) of dichlorobis(trimethylphosphine)nickel(II), 91.4 mg (0.5 mmol) of ethyl 2-chlorobenzoate, 152 mg (1.0 mmol) of cesium fluoride, 140 mg (0.55 mmol) of pinacol bis(borate), 180 mg (1.05 mmol) of trimethyl(2,2,2-trifluoroethoxy)silane, and 0.5 mL of tetrahydrofuran were successively added to the reaction vessel. methyl(2,2,2-trifluoroethoxy)silane and 0.5 mL of tetrahydrofuran, and the reaction vessel was sealed. The reaction mixture was stirred at 100 °C for 2 hours. After completion of the reaction, the reaction vessel was cooled to room temperature and the reaction was quenched by adding 1 mL of saturated aqueous ammonium chloride solution. The reaction mixture was extracted three times with 8 mL of ethyl acetate and the organic phases were combined. The solvent was removed by concentration under reduced pressure and the residue was purified by silica gel column chromatography (eluent ratio: hexane:chloroform:ethyl acetate=16:4:0~16:4:1) to give 107 mg of the white solid product, ethyl 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate, in 78% yield.

References[1] Organic Letters, 2011, vol. 13, # 21, p. 5766 - 5769
[2] Patent: JP5699037, 2015, B2. Location in patent: Paragraph 0083; 0084
2-Ethoxycarbonylphenylboronic acid pinacol ester Preparation Products And Raw materials
Raw materialsEthanol-->Dichloromethane-->Thionyl chloride-->Triethylamine-->Acetonitrile-->1,4-Dioxane-->[1,1'-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)-->2-Iodobenzoic acid-->Pinacolborane-->Ethyl 2-iodobenzoate
Tag:2-Ethoxycarbonylphenylboronic acid pinacol ester(269409-99-6) Related Product Information
2-Phenoxyethanol Emamectin benzoate Diethyl phthalate Pinacol Methyl acrylate Phenoxybenzamine hydrochloride Sodium benzoate Tamoxifen Tris(trimethylsilyl)phosphate Denatonium Benzoate N-Carbobenzyloxyglycine Benzyl benzoate Ethylparaben Ethyl acetate Phenylboronic acid Ethanol Diethyl ether 2-Methoxycarbonylphenylboronic acid