METHYL 2-CHLORO-3-NITROBENZOATE
METHYL 2-CHLORO-3-NITROBENZOATE Basic information
- Product Name:
- METHYL 2-CHLORO-3-NITROBENZOATE
- Synonyms:
-
- METHYL 2-CHLORO-3-NITROBENZOATE
- Benzoic acid, 2-chloro-3-nitro-, methyl ester
- CAS:
- 53553-14-3
- MF:
- C8H6ClNO4
- MW:
- 215.59
- Product Categories:
-
- Aromatic Esters
- Mol File:
- 53553-14-3.mol
METHYL 2-CHLORO-3-NITROBENZOATE Chemical Properties
- Melting point:
- 70 °C
- Boiling point:
- 319.5±22.0 °C(Predicted)
- Density
- 1.426±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- Appearance
- Light yellow to yellow Solid
METHYL 2-CHLORO-3-NITROBENZOATE Usage And Synthesis
Uses
Methyl 2-Chloro-3-nitrobenzoate is a useful research chemical used in the preparation of benzothiadiazole derivatives as agrochemical microbicides.
Synthesis
67-56-1
3970-35-2
53553-14-3
General procedure for the synthesis of methyl 2-chloro-3-nitrobenzoate from methanol and 2-chloro-3-nitrobenzoic acid: 1. to a solution of 2-chloro-3-nitrobenzoic acid (10.0 g, 49.6 mmol) in methanol (80 mL) was added concentrated sulfuric acid (2.0 mL). 2. The reaction mixture was stirred overnight under reflux conditions. 3. Upon completion of the reaction, the methanol was removed by vacuum concentration. 4. Water was added to the residue and extracted with ethyl acetate. 5. The organic phase was washed sequentially with water, saturated sodium bicarbonate solution and saturated brine. 6. 6. The organic phase was dried with magnesium sulfate. 7. The target compound, methyl 2-chloro-3-nitrobenzoate (10.6 g, 99% yield), was obtained as a white solid by vacuum concentration. 8. The product was characterized by 1H NMR (CDCl3) and HPLC: 1H NMR (CDCl3) δ (ppm): 7.95 (dd, 1H), 7.84 (dd, 1H), 7.48 (t, 1H), 3.98 (s, 3H). HPLC Rt = 11.88 min. 150 × 6.0 mm); mobile phase: 0-20 min, acetonitrile/water = 10/90 to 100/0 (gradient), 20-30 min, acetonitrile/water = 100/0 (isocratic); flow rate: 1 mL/min.
References
[1] Patent: WO2008/51533, 2008, A2. Location in patent: Page/Page column 95
[2] Pesticide Science, 1997, vol. 50, # 4, p. 275 - 282
[3] Patent: EP1982982, 2008, A1. Location in patent: Page/Page column 197
[4] Patent: EP2141150, 2010, A1. Location in patent: Page/Page column 109-110
[5] Patent: KR101511396, 2015, B1. Location in patent: Paragraph 2881-2885
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