Identification | More | [Name]
2,6-DICHLOROPHENYLBORONIC ACID | [CAS]
73852-17-2 | [Synonyms]
2,6-DICHLOROBENZENEBORONIC ACID 2,6-DICHLOROPHENYLBORONIC ACID AKOS BRN-0086 RARECHEM AH PB 0089 2,6-Dichlorophenylboronic 3,6-DICHLOROPHENYLBORONICACID 2,6-Dichlorophenylboronic Acid (contains varying amounts of Anhydride) | [EINECS(EC#)]
672-294-4 | [Molecular Formula]
C6H5BCl2O2 | [MDL Number]
MFCD00064869 | [Molecular Weight]
190.82 | [MOL File]
73852-17-2.mol |
Chemical Properties | Back Directory | [Appearance]
Off-white Cryst | [Melting point ]
153 °C | [Boiling point ]
341.8±52.0 °C(Predicted) | [density ]
1.47±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
Powder | [pka]
7.94±0.58(Predicted) | [color ]
Off-white | [Water Solubility ]
Insoluble in water. | [BRN ]
4802506 | [CAS DataBase Reference]
73852-17-2(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
Xi,Xn | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . R22:Harmful if swallowed. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . S37/39:Wear suitable gloves and eye/face protection . | [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29319090 |
Hazard Information | Back Directory | [Chemical Properties]
Off-white Cryst | [Uses]
Reagent used for palladium-catalyzed stille and suzuki-miyaura cross-couplings, palladium (pd)-catalytized reactions. Reagent used in preparation of common building blocks for pharmaceuticals and agrochemicals. | [Uses]
suzuki reaction | [Synthesis]
(1) Lithiation reaction: Add 50 g of 1,3-dichlorobenzene to a 1000 mL three-necked flask under nitrogen atmosphere and cool to -80 to -60°C. Slowly add 176 mL of n-butyl lithium (n-BuLi) dropwise. Slowly add 176 mL of n-Butyl lithium (n-BuLi) dropwise and keep the reaction temperature between -80 and -50℃. After the dropwise addition, the reaction was continued for 2 hours. (2) Lithium-hydrogen exchange reaction: 117 g of tributyl borate (B(OBu)3) was added dropwise to the phenyl lithium solution prepared above, and the reaction temperature was maintained at a holding temperature after the dropwise addition was completed. At the end of the reaction, 10% hydrochloric acid solution was added to the system for acidification, stirred and left to stratify. The organic layers were separated, combined and the solvent was removed, and treated with hydrated succinamide to obtain 51.7 g of crude 2,6-dichlorophenylboronic acid in 80% yield. (3) Purification step: 51.7 g of crude 2,6-dichlorophenylboronic acid was placed in a 1 L three-necked flask and dissolved by adding 200 mL of methyl tert-butyl ether (MTBE). After removing the solvent, cooled and crystallized, centrifuged to obtain 48.4 g of pure 2,6-dichlorophenylboronic acid in 75% yield. | [References]
[1] Patent: CN108084217, 2018, A. Location in patent: Paragraph 0006; 0017-0020; 0022-0024; 0026-0028; 0030-0032 |
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