HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238921Erstellt: 25. Oktober 2026
Ethyl 2-chloropropionate → Ethyl 2-(3-fluoro-4-nitrophenyl)propanoate
https://huagongshe.com/reaction/238921
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl 2-chloropropionate | HCID 10807 | — |
| Edukt | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Ethyl 2-(3-fluoro-4-nitrophenyl)propanoate | HCID 12879863 | 68% |
Reaktionsschritte
To a stirred solution of potassium t-butoxide (20 mmol) in DMF (20 mL) was added a mixture of 2-fluoro-nitrobenzene (10 mmol) and ethyl-2-chloropropionate (10 mmol) at 0° C. dropwise. After being stirred for 10 min at 0° C., the mixture was quenched by 1 N HCl solution, diluted with water and extracted with diethyl ether several times. The combined organic layers were washed with water and brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using EtOAc:hexanes (1:10) as eluant to afford ethyl 2-(3-fluoro-4-nitrophenyl)propionate (1-1, SU-654).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08642657B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-0fbf866d9f15456097d65ecc3742a89a |
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| Quellennotiz | uspto-grants-2014_02 |
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