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2-Methoxy-6-methylbenzoic acid ethyl ester

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2-Methoxy-6-methylbenzoic acid ethyl ester Basic information
Product Name:2-Methoxy-6-methylbenzoic acid ethyl ester
Synonyms:ETHYL 2-METHOXY-6-METHYLBENZOATE;Methoxymethylbenzoicacidethylester;2-Methyl-6-methoxybenzoic acid ethyl ester;2-Methoxy-6-methylbenzoic acid ethyl ester ,95%;M**2-METHOXY-6-METHYLBENZOIC ACID ETHYL ESTER;Ethyl2-Methoxy-6-methylbenzoate>;Benzoic acid, 2-methoxy-6-methyl-, ethyl ester;2-Methoxy-6-methylbenzoic acid ethyl ester
CAS:6520-83-8
MF:C11H14O3
MW:194.23
EINECS:
Product Categories:
Mol File:6520-83-8.mol
2-Methoxy-6-methylbenzoic acid ethyl ester Structure
2-Methoxy-6-methylbenzoic acid ethyl ester Chemical Properties
Boiling point 135 °C / 15mmHg
density 1,09 g/cm3
refractive index 1.5100 to 1.5130
storage temp. Sealed in dry,Room Temperature
form clear liquid
color Colorless to Light yellow to Light orange
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
HS Code 29189900
MSDS Information
2-Methoxy-6-methylbenzoic acid ethyl ester Usage And Synthesis
Synthesis
6-METHYLSALICYLIC ACID ETHYL ESTER

6555-40-4

Iodomethane

74-88-4

2-METHOXY-6-METHYLBENZOIC ACID ETHYL ESTER

6520-83-8

Ethyl 2-hydroxy-6-methylbenzoate (1.0 g, 5.6 mmol), iodomethane (866 mg, 6.1 mmol), and potassium carbonate (1.5 g, 11.1 mmol) were dissolved in acetone (20 mL) and the reaction was heated to reflux for 17 hours. Upon completion of the reaction, the reaction was quenched by adding water (20 mL) to the reaction mixture and extracted with dichloromethane (3 × 20 mL). The organic layers were combined, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography (eluent: 100% hexane) to afford ethyl 2-methoxy-6-methylbenzoate (1.1 g, 99% yield) as a colorless oil.

References[1] Tetrahedron, 1991, vol. 47, # 40, p. 8635 - 8652
[2] Patent: KR101777971, 2017, B1. Location in patent: Paragraph 0138-0139
[3] Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1986, vol. 25, p. 796 - 798
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