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ChemicalBook CAS DataBase List Methyl 3-formyl-2-nitrobenzoate

Methyl 3-formyl-2-nitrobenzoate synthesis

4synthesis methods
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Yield:138229-59-1 85.2%

Reaction Conditions:

with 4-methyl-4-oxidomorpholin-4-ium in acetonitrile at 20; for 16 h;Molecular sieve;

Steps:

1 Compound 3:

Under the condition of 20, NMO (N-methylmorpholine-N-oxide) (85.5g, 730mmol, 77.0mL) was added in batches to the CH3CN (650mL) solution of compound 2 (100g, 365mmol, 1.00eq) , 2.00eq), the addition is completed within 30min, and then 4A molecular sieve (100g, 365mmol, 1.00eq) is added. The reaction mixture was stirred at 20°C for 16 h. TLC (petroleum ether: ethyl acetate=3:1, product: Rf=0.4) showed that the reaction was complete. The reaction solution was suction filtered, and the filter cake was washed three times with CH3CN (200 mL×3). The filtrate was added to water (1000 mL) and extracted. The aqueous phase was back-extracted twice with EtOAc (200 mL x 2), the organic phase was extracted with saturated brine, then the organic phase was dried over anhydrous Na2SO4, filtered with suction, and the filtrate was concentrated under vacuum. The residue was purified by a chromatographic column (SiO2, petroleum ether/ethyl acetate=100/10/1). Compound 3 (65.0 g, 311 mmol, yield 85.2%) was obtained as a pale white solid.

References:

CN112300074,2021,A Location in patent:Paragraph 0035; 0040-0041

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