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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methoxy-4-nitrophenol | HCID 76738 | — |
| Reactant | Methyl 4-bromo-3-methylbutanoate | HCID 14104192 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-methyl-4-(2-methoxy-5-nitrophenoxy)butyrate | HCID 18433387 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06441012B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-567cb79db0824821a119fb0e7f4831ce |
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| Source note | uspto-grants-2002_08 |
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