HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 450117Erstellt: 25. Oktober 2026
Dimethylformamide → N-(2-Fluoro-4-methylsulfanyl-phenyl)-malonamic acid methyl ester
https://huagongshe.com/reaction/450117
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methylmalonylchloride | HCID 10931669 | — |
| Edukt | 2-Fluoro-4-(methylsulfanyl)aniline | HCID 22025617 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Produkt | N-(2-Fluoro-4-methylsulfanyl-phenyl)-malonamic acid methyl ester | HCID 67234589 | 72% |
Reaktionsschritte
To a solution of 2-fluoro-4-methylsulfanylphenylamine (13 g, 82.7 mmol), triethylamine (9.3 mL, 86.8 mmol) and DMAP (100 mg, 0.8 mmol) in DMF (50 mL) was added methyl malonyl chloride (11.5 mL, 82.7 mmol). The reaction was heated at 60° C. for 2 hours then concentrated in vacuo. The resultant residue was dissolved in ethyl acetate (30 mL), washed with water (20 mL) and the aqueous fraction extracted twice with ethyl acetate (2×10 mL). The combined organic fractions were washed with brine, dried (MgSO4) and concentrated in vacuo. The resultant residue was subjected to flash chromatography (SiO2, gradient 10-30% ethylacetate in cyclohexane) to yield the title compound as a white solid (15.4 g, 72%). LCMS (Method B): RT=2.94 min, M+H+=258.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08486963B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-f1140ba2357f4cc68ce82a53e0a0b701 |
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| Quellennotiz | uspto-grants-2013_07 |
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