Identification | More | [Name]
3,5-Dichloro-4-methylbenzoic acid | [CAS]
39652-34-1 | [Synonyms]
3,5-Dichloro-4-methylbenzoic acid | [EINECS(EC#)]
815-608-9 | [Molecular Formula]
C8H6Cl2O2 | [MDL Number]
MFCD09743850 | [Molecular Weight]
205.038 | [MOL File]
39652-34-1.mol |
Chemical Properties | Back Directory | [Melting point ]
187-189 °C(Solv: hexane (110-54-3)) | [Boiling point ]
330.9±37.0 °C(Predicted) | [density ]
1.442±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
3.63±0.10(Predicted) | [color ]
White to Off-White | [InChI]
InChI=1S/C8H6Cl2O2/c1-4-6(9)2-5(8(11)12)3-7(4)10/h2-3H,1H3,(H,11,12) | [InChIKey]
GBEJAEMDMASLJL-UHFFFAOYSA-N | [SMILES]
C(O)(=O)C1=CC(Cl)=C(C)C(Cl)=C1 | [CAS DataBase Reference]
39652-34-1(CAS DataBase Reference) | [EPA Substance Registry System]
Benzoic acid, 3,5-dichloro-4-methyl- (39652-34-1) |
Hazard Information | Back Directory | [Synthesis]
To a 1000 mL four-neck reaction flask (equipped with a mechanical stirrer, thermometer, dropping funnel, and reflux condenser) was added 136 g of p-toluic acid followed by 272 g of dichloroacetic acid as a solvent. Next, 0.2 g of sodium tungstate dihydrate was added as catalyst and 365 g of 30% hydrochloric acid was added. Stirring was initiated and the reaction mixture was heated to 50-60 °C. At this temperature, 136 g of 30% hydrogen peroxide was slowly added dropwise, and the dropwise process was controlled to be completed within 6 hours, during which the temperature was maintained at 50-60 °C. After the dropwise addition, the reaction was continued for 4 hours. The reaction mixture was analyzed by high performance liquid chromatography (HPLC) and the remaining content of p-toluic acid was confirmed to be 9.5%. After completion of the reaction, the reaction solution was distilled under reduced pressure. When no fraction evaporated, the temperature was lowered to 20-30 °C, 250 g of methanol was added, heated to reflux and then cooled to 10 °C again. The reaction mixture was filtered, the solid residue was collected and the filter cake was washed with methanol. The filter cake was dried to give a final product of 165.2 g of 3,5-dichloro-4-methylbenzoic acid in 80.6% yield and 98.5% HPLC purity. | [References]
[1] Patent: US5254584, 1993, A [2] Patent: US5304572, 1994, A [3] Patent: CN105859549, 2016, A. Location in patent: Paragraph 0006; 0011-0012 [4] Organic Process Research and Development, 1999, vol. 3, # 1, p. 10 - 16 |
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