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6520-83-8

6520-83-8 Structure

6520-83-8 Structure
IdentificationBack Directory
[Name]

2-METHOXY-6-METHYLBENZOIC ACID ETHYL ESTER
[CAS]

6520-83-8
[Synonyms]

ETHYL 2-METHOXY-6-METHYLBENZOATE
Methoxymethylbenzoicacidethylester
Ethyl2-Methoxy-6-methylbenzoate>
2-Methyl-6-methoxybenzoic acid ethyl ester
2-METHOXY-6-METHYLBENZOIC ACID ETHYL ESTER
M**2-METHOXY-6-METHYLBENZOIC ACID ETHYL ESTER
Benzoic acid, 2-methoxy-6-methyl-, ethyl ester
2-Methoxy-6-methylbenzoic acid ethyl ester ,95%
[Molecular Formula]

C11H14O3
[MDL Number]

MFCD00191666
[MOL File]

6520-83-8.mol
[Molecular Weight]

194.23
Chemical PropertiesBack Directory
[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 DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[HS Code ]

29189900
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Diethyl ether-->Sulfuric acid-->Tetrahydrofuran-->Acetic acid-->Thionyl chloride-->Magnesium sulfate-->Sodium bicarbonate-->n-Butyllithium-->Carbon dioxide-->Iodine-->Periodic acid-->3-Methylanisole-->1-Methoxy-1,3-cyclohexadiene-->6-Methylsalicylic acid ethyl ester-->Ethyl crotonate
Spectrum DetailBack Directory
[Spectrum Detail]

2-METHOXY-6-METHYLBENZOIC ACID ETHYL ESTER(6520-83-8)1HNMR
Hazard InformationBack Directory
[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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