Methyl 2,3-dichlorobenzoate

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Methyl 2,3-dichlorobenzoate manufacturers

Methyl 2,3-dichlorobenzoate Basic information
Product Name:Methyl 2,3-dichlorobenzoate
Synonyms:2,3-DICHLOROBENZOIC ACID METHYL ESTER;RARECHEM AL BF 0205;Methyl 2,3-dichlorobenzoate,97%;2,3-Dichlorobenzoic methylester;Methyl 2,3-dichlorobenzoate,98+%;Benzoic acid, 2,3-dichloro-, Methyl ester;2,3-dichloro-benzoicacimethylester;Methyl 2,3-dichlorobenzoate , 2,3-Dichlorobenzoic acid methyl ester
CAS:2905-54-6
MF:C8H6Cl2O2
MW:205.04
EINECS:
Product Categories:Aromatic Esters
Mol File:2905-54-6.mol
Methyl 2,3-dichlorobenzoate Structure
Methyl 2,3-dichlorobenzoate Chemical Properties
Melting point 33-38 °C
Boiling point 294.45°C (rough estimate)
density 1.36
refractive index 1.5537
Fp 110 °C
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
color White to Off-White
EPA Substance Registry SystemBenzoic acid, 2,3-dichloro-, methyl ester (2905-54-6)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 37/39-26
TSCA TSCA listed
HS Code 29163900
MSDS Information
ProviderLanguage
ACROS English
Methyl 2,3-dichlorobenzoate Usage And Synthesis
Chemical Propertieswhite crystals
Synthesis
2,3-Dichlorobenzoic acid

50-45-3

METHYL 2,3-DICHLOROBENZOATE

2905-54-6

a) 2,3-Dichlorobenzoic acid (100 g, 0.526 mol) was dissolved in methanol (1 L) and concentrated sulfuric acid (20 mL) was added slowly. The reaction mixture was stirred under reflux conditions for 12 hours. After completion of the reaction, it was cooled to room temperature and concentrated under reduced pressure to remove most of the solvent. The residue was diluted with ethyl acetate (1 L) and water (100 mL) and the organic layer was separated. The organic phase was washed sequentially with saturated sodium bicarbonate solution and brine and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure to afford methyl 2,3-dichlorobenzoate (99 g, 92% yield) as a white solid.1H NMR (300 MHz, CDCl3) δ ppm: 3.95 (s, 3H), 7.27 (t, J = 7.8 Hz, 1H), 7.60 (dd, J = 1.8, 7.8 Hz, 1H), 7.66 (dd, J = 1.8, 7.8 Hz, 1H).

References[1] Patent: WO2013/28263, 2013, A1. Location in patent: Page/Page column 78
[2] Patent: US9096605, 2015, B2
[3] Patent: EP459830, 1991, A1
Methyl 2,3-dichlorobenzoate Preparation Products And Raw materials
Raw materials2,3-Dichlorobenzoic acid-->Sulfuric acid-->Methanol
Preparation Products2,3-Dichlorobenzyl bromide-->2,3-Dichlorophenylacetonitrile
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