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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 2-chloropropionateHCID 10807—
Edukt1-Fluoro-2-nitrobenzeneHCID 73895—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl 2-(3-fluoro-4-nitrophenyl)propanoateHCID 1287986368%

Reaktionsbedingungen

Temperatur0 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642657B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-0fbf866d9f15456097d65ecc3742a89a
Quellennotizuspto-grants-2014_02