3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID
3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID Basic information
- Product Name:
- 3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID
- Synonyms:
-
- RARECHEM AL BO 1012
- 3-TRIFLUOROMETHYL-5-NITROBENZOIC ACID
- 3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID
- 3-CARBOXY-5-NITROBENZOTRIFLUORIDE
- A,A,A-TRIFLUORO-5-NITRO-M-TOLUIC ACID
- LABOTEST-BB LT00454389
- BUTTPARK 25\01-30
- 5-(Trifluoromethyl)-3-nitrobenzoic acid
- CAS:
- 328-80-3
- MF:
- C8H4F3NO4
- MW:
- 235.12
- EINECS:
- 630-023-7
- Product Categories:
-
- Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
- Benzoic acid
- Mol File:
- 328-80-3.mol
3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID Chemical Properties
- Melting point:
- 128 °C
- Boiling point:
- 309.9±42.0 °C(Predicted)
- Density
- 1.596±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- form
- powder to crystal
- pka
- 3.05±0.10(Predicted)
- color
- White to Light yellow to Light orange
- BRN
- 2284651
- CAS DataBase Reference
- 328-80-3(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39-60-37
- HazardClass
- IRRITANT
- HS Code
- 29163990
MSDS
- Language:English Provider:ALFA
3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID Usage And Synthesis
Synthesis
454-92-2
328-80-3
The general procedure for synthesizing 3-nitro-5-(trifluoromethyl)benzoic acid from 3-trifluoromethylbenzoic acid is as follows: 1. 90% fuming nitric acid (210 mL) was slowly added to a solution of concentrated sulfuric acid (880 mL) of 3-trifluoromethylbenzoic acid (203.4 g) at 0 °C, and the addition process continued for 1 hour. 2. the reaction mixture was stirred at 35°C for 3 hours. 3. The reaction solution was slowly poured into ice (about 1 kg) to precipitate the product. 4. The precipitate was collected by filtration and washed with water (500 mL). 5. The precipitate was dissolved in ethyl acetate (500 mL) and the organic phase was washed with water. 6. After drying the organic phase, the solvent was evaporated under reduced pressure to give 3-nitro-5-(trifluoromethyl)benzoic acid (232.5 g, 92% yield) as a white powder. 1H-NMR (300MHz, CDCl3): δ 8.69 (1H, s), 8.74 (1H, s), 9.1 (1H, s).
References
[1] Patent: US2008/275085, 2008, A1. Location in patent: Page/Page column 45
[2] Journal of the American Chemical Society, 2017, vol. 139, # 43, p. 15308 - 15311
[3] Journal of Medicinal Chemistry, 2016, vol. 59, # 6, p. 2362 - 2380
[4] Angewandte Chemie - International Edition, 2017, vol. 56, # 8, p. 2059 - 2063
[5] Angew. Chem., 2017, vol. 129, # 8, p. 2091 - 2095,5
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