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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305629Generated: November 1, 2026

Potassium Carbonate → Methyl 3-methyl-4-(2-methoxy-5-nitrophenoxy)butyrate

https://huagongshe.com/reaction/2305629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methoxy-4-nitrophenolHCID 76738—
ReactantMethyl 4-bromo-3-methylbutanoateHCID 14104192—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-methyl-4-(2-methoxy-5-nitrophenoxy)butyrateHCID 18433387—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-methoxy-4-nitrophenol (0.207 mg. 1.23 mmole) {Aldrich}, methyl 4-bromo-3-methylbutyrate(0.25 g. 1.35 mmole) and potassium carbonate (0.19 g. 1.35 mmole) in DMF (10 mL.) was heated and stirred at 80° C. for 8 hours. After cooling, the inorganics were filtered off, and the filtrate evaporated to dryness. The residue was dissolved in dichloromethane and washed twice with water. After drying (MgSO4) the solvent was evaporated off to yield an oil. The oil was purified by chromatography (Varian Megabondelut silica column) using a gradient of 100% dichloromethane to 20% ethyl acetate/dichloromethane to give methyl 3-methyl-4-(2-methoxy-5-nitrophenoxy)butyrate as an oil (90 mg. 29%) ms 284(M+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441012B1
Source datasetuspto-grants-2002_08
ORD IDord-567cb79db0824821a119fb0e7f4831ce
Source noteuspto-grants-2002_08