Methyl 2-bromo-6-methylbenzoate

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CAS:99548-56-8
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Purity:98% Package:g-Kg Remarks:Colorless to pale yellow liquid
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Methyl 2-bromo-6-methylbenzoate manufacturers

Methyl 2-bromo-6-methylbenzoate Basic information
Product Name:Methyl 2-bromo-6-methylbenzoate
Synonyms:2-BROMO-6-METHYLBENZOIC ACID METHYL ESTER;Methyl 2-bromo-6-methylbenzoate;Methyl 6-bromo-o-toluate, 3-Bromo-2-(methoxycarbonyl)toluene;Benzoic acid, 2-broMo-6-Methyl-, Methyl ester
CAS:99548-56-8
MF:C9H9BrO2
MW:229.07
EINECS:
Product Categories:Pharmaceutical intermediate;Aromatic Esters
Mol File:99548-56-8.mol
Methyl 2-bromo-6-methylbenzoate Structure
Methyl 2-bromo-6-methylbenzoate Chemical Properties
Boiling point 141 °C(Press: 21 Torr)
density 1.433±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
AppearanceColorless to light yellow Liquid
InChIInChI=1S/C9H9BrO2/c1-6-4-3-5-7(10)8(6)9(11)12-2/h3-5H,1-2H3
InChIKeyDDJSNWUTQDNGIZ-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=C(C)C=CC=C1Br
Safety Information
HS Code 2916399090
MSDS Information
Methyl 2-bromo-6-methylbenzoate Usage And Synthesis
Synthesis
Methanol

67-56-1

2-Bromo-6-methylbenzoic acid

90259-31-7

Methyl 2-bromo-6-methylbenzoate

99548-56-8

To a dichloromethane (50 mL) suspension of 2-bromo-6-methylbenzoic acid (5.05 g, 23.48 mmol) was sequentially added oxalyl chloride (2.67 mg, 30.5 mmol) and N,N-dimethylformamide (DMF, 2 drops) at room temperature. The reaction mixture was stirred at room temperature for 2 hours and then concentrated under reduced pressure to remove the solvent. Methanol (10 mL) was added to the resulting residue and stirring was continued overnight. Upon completion of the reaction, the reaction mixture was concentrated under reduced pressure. To the concentrated residue was added saturated aqueous sodium bicarbonate (20 mL) and the mixture was extracted with ethyl acetate. The organic layer was dried with anhydrous magnesium sulfate and the solvent was removed under reduced pressure. The resulting methyl 2-bromo-6-methylbenzoate (5.04 g, 94% yield) was used directly in the subsequent reaction without further purification.

References[1] Patent: EP2455370, 2012, A1. Location in patent: Page/Page column 101
[2] Patent: WO2007/47646, 2007, A2. Location in patent: Page/Page column 52
Methyl 2-bromo-6-methylbenzoate Preparation Products And Raw materials
Raw materialsMethanol-->2-Bromo-6-methylbenzoic acid-->Dichloromethane-->Oxalyl chloride
Tag:Methyl 2-bromo-6-methylbenzoate(99548-56-8) Related Product Information
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