4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER manufacturers
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| | 4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER Basic information |
| Product Name: | 4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER | | Synonyms: | 4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER;4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-BENZAMIDE;4-(tetraMethyl-1,3,2-dioxaborolan-2-yl)benzaMide;Benzamide, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-;4-Carbamoylphenylboronic Acid Pinacol Ester;4-Carbamoylbenzeneboronic acid pinacol ester | | CAS: | 179117-44-3 | | MF: | C13H18BNO3 | | MW: | 247.1 | | EINECS: | | | Product Categories: | blocks;BoronicAcids;Carboxes;Heterocyclic Compounds | | Mol File: | 179117-44-3.mol |  |
| | 4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER Chemical Properties |
| Melting point | 174.9-180.3 °C | | Boiling point | 388.2±25.0 °C(Predicted) | | density | 1.11±0.1 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | form | solid | | pka | 15.86±0.50(Predicted) | | color | White | | InChI | 1S/C13H18BNO3/c1-12(2)13(3,4)18-14(17-12)10-7-5-9(6-8-10)11(15)16/h5-8H,1-4H3,(H2,15,16) | | InChIKey | NWEMAGLLVQDEKL-UHFFFAOYSA-N | | SMILES | B2(OC(C(O2)(C)C)(C)C)c1ccc(cc1)C(=O)N | | CAS DataBase Reference | 179117-44-3(CAS DataBase Reference) |
| Hazard Codes | Xn | | Risk Statements | 22 | | WGK Germany | 3 | | HS Code | 2931900090 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral |
| | 4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER Usage And Synthesis |
| Synthesis | Under argon protection, 1.4 mg (0.005 mmol) of dichlorobis(trimethylphosphine)nickel (NiCl2(PMe3)2), 77.4 mg (0.5 mmol) of 4-chlorobenzamide, 152 mg (1.0 mmol) of cesium fluoride (CsF), 140 mg (0.55 mmol) of bis(pinacolato)bis(boronic acid) ( B2pin2), 180 mg (1.05 mmol) trimethyl (2,2,5,5-tetrafluoroethoxy) silane (TMSEF), and 0.5 mL 1,4-dioxane. The reaction vessel was sealed and the mixture was stirred and reacted at 100°C for 12 hours. Upon completion of the reaction, the reaction vessel was cooled to room temperature and the reaction was quenched by the addition of 1 mL of saturated aqueous ammonium chloride. The mixture was extracted three times with 8 mL of ethyl acetate and the organic phases were combined. The solvent was removed by distillation under reduced pressure and the residue was purified by silica gel column chromatography (eluent gradient: hexane/chloroform/ethyl acetate = 4:1:0 to 4:1:1) to afford 92 mg (75% yield) of the target product 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide as a white solid. | | References | [1] Organic and Biomolecular Chemistry, 2014, vol. 12, # 22, p. 3604 - 3610 [2] Organic Letters, 2011, vol. 13, # 21, p. 5766 - 5769 [3] Patent: JP5699037, 2015, B2. Location in patent: Paragraph 0091; 0092 |
| | 4-AMINOCARBONYLPHENYLBORONIC ACID, PINACOL ESTER Preparation Products And Raw materials |
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