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70163-98-3

70163-98-3 Structure

70163-98-3 Structure
IdentificationBack Directory
[Name]

3-FLUORO-2-HYDROXY-BENZOIC ACID METHYL ESTER
[CAS]

70163-98-3
[Synonyms]

RARECHEM AL BF 0031
Methyl 3-fluorosalicylate
3-Fluorosalicylic acid methyl ester
3-FLUORO-2-HYDROXY-BENZOIC ACID METHYL ESTER
Benzoic acid, 3-fluoro-2-hydroxy-, methyl ester
[Molecular Formula]

C8H7FO3
[MDL Number]

MFCD06203651
[MOL File]

70163-98-3.mol
[Molecular Weight]

170.14
Chemical PropertiesBack Directory
[Melting point ]

46-47 °C
[Boiling point ]

211.7±25.0 °C(Predicted)
[density ]

1.309±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

8.50±0.10(Predicted)
[color ]

Off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P280-P301+P312-P305+P351+P338
[HS Code ]

2916399090
Spectrum DetailBack Directory
[Spectrum Detail]

3-FLUORO-2-HYDROXY-BENZOIC ACID METHYL ESTER(70163-98-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

METHYL 3-FLUOROBENZOATE

455-68-5

3-FLUORO-2-HYDROXY-BENZOIC ACID METHYL ESTER

70163-98-3

General procedure for the synthesis of methyl 3-fluoro-2-hydroxy-benzoate from methyl 3-fluorobenzoate: Ru(MesCO2)(L) (p-cymene) [L is 2,2'-pyridine or 4,4'-dibromo bipyridine] (2.5 mol%), oxidizing agent (2.0 eq.) and methyl 3-fluorobenzoate (1.0 eq.) were added to a sealed tube. Subsequently, a solvent mixture of trifluoroacetic acid (TFA) and trifluoroacetic anhydride (TFAA) in the ratio of 0.6 mL:0.4 was added. The reaction mixture was placed in an oil bath preheated to 110 °C with continuous stirring until the reaction was completed, and the reaction process was monitored by thin layer chromatography (TLC). After completion of the reaction, the reaction mixture was quenched by addition of ice water and extracted with dichloromethane. The organic layer was dried with anhydrous sodium sulfate (Na2SO4) and subsequently concentrated by rotary evaporation. Finally, the residue was purified by silica gel column chromatography to afford the target product methyl 3-fluoro-2-hydroxy-benzoate.

[References]

[1] Tetrahedron Letters, 2017, vol. 58, # 38, p. 3743 - 3746
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