ChemicalBook--->CAS DataBase List--->773873-26-0

773873-26-0

773873-26-0 Structure

773873-26-0 Structure
IdentificationBack Directory
[Name]

2,3-DIFLUORO-4-METHOXYBENZOIC ACID
[CAS]

773873-26-0
[Synonyms]

2,3-Difluoro-6-methoxybenzoic acid
2,3-Difluoro-4-methoxylbenzoic acid
Benzoic acid, 2,3-difluoro-6-methoxy-
[Molecular Formula]

C8H6F2O3
[MDL Number]

MFCD03428569
[MOL File]

773873-26-0.mol
[Molecular Weight]

188.13
Chemical PropertiesBack Directory
[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 DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HS Code ]

2918999090
Spectrum DetailBack Directory
[Spectrum Detail]

2,3-DIFLUORO-4-METHOXYBENZOIC ACID(773873-26-0)1HNMR
2,3-DIFLUORO-4-METHOXYBENZOIC ACID(773873-26-0)19FNMR
2,3-DIFLUORO-4-METHOXYBENZOIC ACID(773873-26-0)13CNMR
Hazard InformationBack Directory
[Synthesis]

2,3-DIFLUORO-6-METHOXYBENZALDEHYDE

187543-87-9

2,3-DIFLUORO-4-METHOXYBENZOIC ACID

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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