ChemicalBook--->CAS DataBase List--->7083-19-4

7083-19-4

7083-19-4 Structure

7083-19-4 Structure
IdentificationBack Directory
[Name]

2-METHOXY-5-METHYLBENZALDEHYDE
[CAS]

7083-19-4
[Synonyms]

5-Methyl-2-methoxybenzaldehyde
Benzaldehyde, 2-methoxy-5-methyl-
[Molecular Formula]

C9H10O2
[MDL Number]

MFCD02261770
[MOL File]

7083-19-4.mol
[Molecular Weight]

150.17
Chemical PropertiesBack Directory
[density ]

1.08
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

2-METHOXY-5-METHYLBENZALDEHYDE(7083-19-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-Methylsalicylaldehyde

613-84-3

Iodomethane

74-88-4

2-METHOXY-5-METHYLBENZALDEHYDE

7083-19-4

Step 1: Suspend 5-methylsalicylaldehyde (2-hydroxy-5-methylbenzaldehyde, CAS No. 613-84-3) in a solvent mixture of 5 mL dichloromethane and 5 mL water. 1.47 mL (4.4 mmol, 3 eq.) of 1 N sodium hydroxide solution and 1.52 g (2.94 mmol, 2 eq.) of 50% aqueous tetrabutylammonium hydroxide were added sequentially, followed by iodomethane (457 μL, 5 eq.). The reaction mixture was stirred at room temperature for 3 hours. After completion of the reaction, the reaction mixture was extracted with dichloromethane three times, the organic phases were combined, washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel fast column chromatography (eluent: cyclohexane/ethyl acetate, 9/1, v/v) to afford 215 mg (97% yield) of the target compound 2-methoxy-5-methylbenzaldehyde.

[References]

[1] Canadian Journal of Chemistry, 2012, vol. 90, # 11, p. 965 - 974
[2] Journal of Medicinal Chemistry, 2002, vol. 45, # 19, p. 4188 - 4201
[3] Patent: WO2010/66847, 2010, A1. Location in patent: Page/Page column 70
[4] Indian Journal of Chemistry - Section B Organic Chemistry Including Medicinal Chemistry, 1990, vol. 29, # 9, p. 876 - 878
[5] Beilstein Journal of Organic Chemistry, 2018, vol. 14, p. 734 - 746
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