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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17789Erstellt: 23. Oktober 2026

(E)-1,3-Dichloropropene → N-(3-Chloro-allyl)-2,2,2-trifluoro-acetamide

https://huagongshe.com/de/reaction/17789

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(E)-1,3-DichloropropeneHCID 24726—
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
EduktTrifluoroacetamideHCID 67717—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(3-Chloro-allyl)-2,2,2-trifluoro-acetamideHCID 86761131—

Reaktionsschritte

Trifluoroacetamide (10.44 g, 92.4 mmol) is dissolved in THF (30 mL). Sodium hydride (60% weight dispersion in mineral oil, 3.1 g, 77 mmol) is then added in small portions at room temperature while regulating the temperature of the reaction with a water bath. The mixture is stirred at room temperature for 5 min., after which E-1,3-dichloropropene (4.5 mL, 49.4 mmol) is added. After 2 min., the mixture thickened, and the reaction was heated to reflux for 45 min. The mixture is then cooled to room temperature, and saturated aqueous ammonium chloride (20 mL) and water (40 mL) are added. The mixture is transferred to a separatory funnel and extracted with ether (2×400 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to obtained a colorless oil that was used for the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741294B1
Quelldatensatzuspto-grants-2010_06
ORD IDord-09f05db54e8449f1b33909fca330bb9d
Quellennotizuspto-grants-2010_06