| Identification | Back Directory | [Name]
METHYL 2-FLUORO-4-HYDROXYBENZOATE | [CAS]
197507-22-5 | [Synonyms]
METHYL 2-FLUORO-4-HYDROXYBENZOATE
Methyl2-fluoro-4-hydroxybenzoate,98%
Methyl 2-fluoro-4-hydroxybenzoate 98%
2-Fluoro-4-hydroxybenzoic acid methyl ester
BENZOIC ACID, 2-FLUORO-4-HYDROXY-, METHYL ESTER | [Molecular Formula]
C8H7FO3 | [MDL Number]
MFCD09038282 | [MOL File]
197507-22-5.mol | [Molecular Weight]
170.138 |
| Chemical Properties | Back Directory | [Boiling point ]
287℃ | [density ]
1.309 | [Fp ]
127℃ | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [form ]
crystalline powder | [pka]
7.36±0.18(Predicted) | [color ]
Off white to faint gold | [Water Solubility ]
Slightly soluble in water. | [InChI]
InChI=1S/C8H7FO3/c1-12-8(11)6-3-2-5(10)4-7(6)9/h2-4,10H,1H3 | [InChIKey]
WYSPMXSNCAFCFV-UHFFFAOYSA-N | [SMILES]
C(OC)(=O)C1=CC=C(O)C=C1F |
| Hazard Information | Back Directory | [Uses]
Methyl 2-fluoro-4-hydroxybenzoate can be used in the preparation of compounds, with the ability to inhibit cytosolic phospholipase A2α. It is also an intermediate in the synthesis of 3-(2-fluoro-4-hydroxyphenyl)-5-(trifluoromethyl) -4-isoxazolecarboxylic acid methyl ester (F591865). | [Synthesis]
General procedure for the synthesis of methyl 2-fluoro-4-hydroxybenzoate from methanol and 2-fluoro-4-hydroxybenzoic acid: Referring to Example 10 of the literature; 2-fluoro-4-hydroxybenzoic acid (50.0 g) was dissolved in methanol (700 mL), concentrated sulfuric acid (10 mL) was added as a catalyst, and the reaction was carried out with heating and stirring for 16 hrs. at 90 °C. After the reaction was completed, the reaction solution was concentrated, and the resulting colorless crystals were washed with water and dried to obtain the target product methyl 2-fluoro-4-hydroxybenzoate (51 g, 94% yield) as colorless crystals. The product was characterized by 1H NMR (300 MHz, DMSO-d6): δ 3.79 (3H, s), 6.61-6.72 (2H, m), 7.73-7.79 (1H, m), 10.80 (1H, br). | [References]
[1] Patent: EP2392573, 2011, A1. Location in patent: Page/Page column 39
[2] Patent: EP2522657, 2012, A1. Location in patent: Page/Page column 36-37
[3] Patent: WO2010/45258, 2010, A2. Location in patent: Page/Page column 140; 141
[4] Patent: WO2009/111056, 2009, A1. Location in patent: Page/Page column 212
[5] ChemMedChem, 2013, vol. 8, # 5, p. 779 - 799 |
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