2,3-DIFLUORO-4-METHOXYBENZOIC ACID
2,3-DIFLUORO-4-METHOXYBENZOIC ACID Basic information
- Product Name:
- 2,3-DIFLUORO-4-METHOXYBENZOIC ACID
- Synonyms:
-
- 2,3-Difluoro-4-methoxylbenzoic acid
- 2,3-Difluoro-6-methoxybenzoic acid
- Benzoic acid, 2,3-difluoro-6-methoxy-
- CAS:
- 773873-26-0
- MF:
- C8H6F2O3
- MW:
- 188.13
- Product Categories:
-
- Aromatic Halides (substituted)
- Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
- Benzoic acid
- Mol File:
- 773873-26-0.mol
2,3-DIFLUORO-4-METHOXYBENZOIC ACID Chemical Properties
- Melting point:
- 126-129°C
- Boiling point:
- 275.0±35.0 °C(Predicted)
- Density
- 1.399±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 2.82±0.10(Predicted)
Safety Information
- Hazard Codes
- Xi
- Hazard Note
- Irritant
- HS Code
- 2918999090
2,3-DIFLUORO-4-METHOXYBENZOIC ACID Usage And Synthesis
Synthesis
187543-87-9
773873-26-0
General procedure for the synthesis of 2,3-difluoro-6-methoxybenzoic acid from 2,3-difluoro-6-methoxybenzaldehyde: 1. Preparation of reaction system: 2,3-difluoro-6-methoxybenzaldehyde (0.5 g, 2.91 mmol) was suspended in potassium hydroxide solution (3 g KOH dissolved in 20 ml of water). 2. Oxidizing reaction: hydrogen peroxide solution (27.5% w/w, 4 ml) was added to the above suspension, followed by heating the reaction at 70°C for 2 hours. 3. Acidification: after completion of the reaction, the reaction mixture was acidified to pH 2 with concentrated hydrochloric acid. 4. Extractive separation: the acidified reaction mixture was washed with ethyl acetate. 5. Drying and concentration: the organic phases were combined, dried with anhydrous magnesium sulfate, filtered and the solvent was evaporated in vacuum. 6. Purification: Further purification by azeotropy with toluene afforded 2,3-difluoro-6-methoxybenzoic acid as a white solid (500 mg, 91% yield). Remarks: LC/MS analysis showed a retention time of 12.08 min and no molecular ion peak was observed.
References
[1] Patent: WO2006/77414, 2006, A1. Location in patent: Page/Page column 148
[2] Patent: CN105523921, 2016, A. Location in patent: Paragraph 0014; 0015; 0016
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