METHYL 4-BROMO-2-HYDROXYBENZOATE

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METHYL 4-BROMO-2-HYDROXYBENZOATE manufacturers

METHYL 4-BROMO-2-HYDROXYBENZOATE Basic information
Product Name:METHYL 4-BROMO-2-HYDROXYBENZOATE
Synonyms:Methyl 4-bromo-2-hydroxybenzenecarboxylate;4-Bromo-2-hydroxybenzoic acid methyl ester;Benzoic acid, 4-bromo-2-hydroxy-, methyl ester;Methyl 4-Bromosalicylate;Methyl 4-bromo-2-hydroxybenzoate
CAS:22717-56-2
MF:C8H7BrO3
MW:231.04
EINECS:
Product Categories:Aromatic Esters;Acids & Esters;Bromine Compounds;Phenols
Mol File:22717-56-2.mol
METHYL 4-BROMO-2-HYDROXYBENZOATE Structure
METHYL 4-BROMO-2-HYDROXYBENZOATE Chemical Properties
Melting point 41-42°
Boiling point 284.7±20.0 °C(Predicted)
density 1.627±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka8.79±0.10(Predicted)
form solid
AppearanceWhite to yellow Solid
InChIInChI=1S/C8H7BrO3/c1-12-8(11)6-3-2-5(9)4-7(6)10/h2-4,10H,1H3
InChIKeyJEMVEVUWSJXZMX-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC=C(Br)C=C1O
Safety Information
WGK Germany WGK 3
HazardClass IRRITANT
HS Code 2916310090
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Oral
MSDS Information
METHYL 4-BROMO-2-HYDROXYBENZOATE Usage And Synthesis
Synthesis
Methanol

67-56-1

4-Bromo-2-hydroxybenzoic acid

1666-28-0

METHYL 4-BROMO-2-HYDROXYBENZOATE

22717-56-2

2-Hydroxy-4-bromobenzoic acid (5.0 g, 23.1 mmol) was dissolved in 20 mL of anhydrous methanol and 1.7 mL of concentrated sulfuric acid was added slowly. The reaction mixture was heated and refluxed under stirring for 24 hours. Upon completion of the reaction, the reaction solution was poured into ice water and concentrated by rotary evaporator to remove methanol. Subsequently, extraction was carried out with ethyl acetate (EA) and the organic phase was washed with saturated sodium bicarbonate (NaHCO3) solution and dried over anhydrous sodium sulfate. Finally, the organic phase was concentrated to afford methyl 2-hydroxy-4-bromobenzoate (5.31 g) as a reddish brown solid, and the product was used directly in the next reaction without further purification.

References[1] Journal of Medicinal Chemistry, 2012, vol. 55, # 7, p. 3228 - 3241
[2] Patent: US2016/221997, 2016, A1. Location in patent: Paragraph 0245; 0246; 0247
[3] Patent: WO2016/115282, 2016, A1. Location in patent: Page/Page column 76
[4] Patent: WO2015/163485, 2015, A1. Location in patent: Paragraph 0372
[5] Tetrahedron Letters, 2016, vol. 57, # 48, p. 5301 - 5303
Tag:METHYL 4-BROMO-2-HYDROXYBENZOATE(22717-56-2) Related Product Information
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