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116119-01-8

116119-01-8 Structure

116119-01-8 Structure
IdentificationBack Directory
[Name]

1,3-Benzodioxole-5-carboxylic acid, 7-hydroxy-, methyl ester
[CAS]

116119-01-8
[Synonyms]

Methyl 3,4-Methylenedioxy-5-hydroxybenzoate
methyl 7-hydroxy-1,3-benzodioxole-5-carboxylate
methyl 7-hydroxy-2H-1,3-benzodioxole-5-carboxylate
Methyl 7-hydroxybenzo[d][1,3]dioxole-5-carboxylate
7-Hydroxy-1,3-benzodioxole-5-carboxylic Acid Methyl Ester
1,3-Benzodioxole-5-carboxylic acid, 7-hydroxy-, methyl ester
[Molecular Formula]

C9H8O5
[MDL Number]

MFCD22123663
[MOL File]

116119-01-8.mol
[Molecular Weight]

196.16
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

CDCl3, DCM, Ethanol, Ethyl Acetate,
[form ]

Solid
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

7-Hydroxy-1,3-benzodioxole-5-carboxylic Acid Methyl Ester is an intermediate in the synthesis of natural dihydrostilbenes with significant cytotoxicity toward human cancer cell lines.
[Synthesis]

Diiodomethane

75-11-6

Methyl gallate

99-24-1

1,3-Benzodioxole-5-carboxylic acid, 7-hydroxy-, methyl ester

116119-01-8

Potassium carbonate (4.002 g, 29 mmol) and methyl gallate (6 g, 29.7 mmol) were dissolved in anhydrous dichloromethane followed by the addition of diiodomethane (2.8 mL, 34.8 mmol) under nitrogen atmosphere and at room temperature. The reaction mixture was stirred at 0 °C for 5 h and then warmed up to 120 °C to continue the reaction. Upon completion of the reaction, the mixture was poured into cooled water (500 mL) and extracted with ethyl acetate. The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (eluent: 15% ethyl acetate/hexane) to afford the target product methyl 7-hydroxybenzo[d][1,3]meso-dioxole-5-carboxylate (3.6 g, 58% yield) as a white amorphous powder.

[References]

[1] Tetrahedron Asymmetry, 2009, vol. 20, # 4, p. 440 - 448
[2] Synlett, 2018, vol. 29, # 7, p. 908 - 911
[3] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 7, p. 2297 - 2298
[4] Liebigs Annalen der Chemie, 1994, # 4, p. 361 - 364
[5] Synthesis, 2009, # 20, p. 3383 - 3390
Spectrum DetailBack Directory
[Spectrum Detail]

1,3-Benzodioxole-5-carboxylic acid, 7-hydroxy-, methyl ester(116119-01-8)1HNMR
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