Molecular Formula | C7H5ClF3N |
Molar Mass | 195.57 |
Density | 1.425±0.06 g/cm3(Predicted) |
Boling Point | 112-115 °C |
Flash Point | 100.6°C |
Vapor Presure | 0.0333mmHg at 25°C |
Appearance | Crystallization |
pKa | 1.71±0.10(Predicted) |
Storage Condition | Keep in dark place,Sealed in dry,2-8°C |
Refractive Index | 1.5 |
MDL | MFCD00278479 |
Hazard Symbols | Xi - Irritant |
Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
UN IDs | 2810 |
Hazard Note | Irritant |
Hazard Class | 6.1 |
Packing Group | Ⅲ |
Application | 4-amino-2-chlorotrifluorotoluene is a pharmaceutical intermediate, which can be used from 1-bromo-2-chloro-4-nitrobenzene as raw material. First prepare 2-chloro-4-nitro-1-trifluoromethylbenzene, and then reduce the nitro to obtain 4-amino-2-chlorotrifluorotoluene. |
preparation | step a, preparation of 2-chloro -4-nitro -1-trifluoromethyl benzene mixed 1-bromo -2-chloro -4-nitrobenzene (1.86g,7.86mmol) and CuI(0.225g,1.18mmol) in anhydrous DMF(50mL) and degassing with N2 for 15 minutes. Methyl fluorosulfonyl difluoroacetate (3.53g,23.6mmol) was added and the mixture was heated at 80°C for 16 hours. After cooling to room temperature, the reaction mixture was divided between ethyl acetate (100mL) and salt water (100mL). The water layer was extracted with additional ethyl acetate (100mL). The combined organics were washed with 3 × 200mL saline, dried with Na2sO4, concentrated and purified by chromatography, eluted with ethyl acetate/hexane (1 ∶ 9). Step B, Preparation of 4-amino-2-chlorotrifluorotoluene At room temperature, tin (II) chloride dihydrate (4.97mmol) was added to a solution of 2-chloro-4-nitro-1-trifluoromethyl benzene (4.14mmol) in methanol at one time and the mixture was stirred for 16 hours. The mixture was vacuum concentrated and purified by chromatography, eluted with ethyl acetate/hexane (1 ∶ 4 to 2 ∶ 3) to give the title compound. |