3-Nitro-5-(trifluoromethyl)benzoic acid

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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-CARBOXY-5-NITROBENZOTRIFLUORIDE;A,A,A-TRIFLUORO-5-NITRO-M-TOLUIC ACID;LABOTEST-BB LT00454389;BUTTPARK 25\01-30;5-(Trifluoromethyl)-3-nitrobenzoic acid;3-Nitro-5-(trifluoromethyl)benzoic acid 97%
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 Structure
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
pka3.05±0.10(Predicted)
color White to Light yellow to Light orange
BRN 2284651
CAS DataBase Reference328-80-3(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 Information
ProviderLanguage
ALFA English
3-Nitro-5-(trifluoromethyl)benzoic acid Usage And Synthesis
Synthesis
3-(Trifluoromethyl)benzoic acid

454-92-2

3-NITRO-5-(TRIFLUOROMETHYL)BENZOIC ACID

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
3-Nitro-5-(trifluoromethyl)benzoic acid Preparation Products And Raw materials
Raw materials3-(Trifluoromethyl)benzoic acid
Preparation Products3-Chloro-5-(trifluoromethyl)benzaldehyde-->3-Amino-5-trifluoromethyl-benzamide
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