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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1967457Erstellt: 26. Oktober 2026

Benzaldehyde, 3-amino- → 1-(2-Fluoro-5-trifluoromethylphenyl)-3-(3-formylphenyl)urea

https://huagongshe.com/reaction/1967457

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehyde, 3-amino-HCID 74366—
EduktPotassium bisulfateHCID 516920—
Edukt2-Fluoro-5-(trifluoromethyl)phenyl isocyanateHCID 2733380—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt1-(2-Fluoro-5-trifluoromethylphenyl)-3-(3-formylphenyl)ureaHCID 8736230257%

Reaktionsschritte

A mixture of 484 mg of 3-aminobenzaldehyde (4 mmol) (polymerized form) and 290 μl of 2-fluoro-5-trifluoromethylphenyl isocyanate in 4 ml of DCE is treated in a CEM Discover microwave oven at 100° C. for 10 minutes (power 90). After cooling, the mixture is poured into 100 ml of saturated potassium hydrogen sulfate solution and extracted with twice 50 ml of ethyl acetate. The combined organic phases are washed with water, dried over sodium sulfate and evaporated. 740 mg of the expected aldehyde (yield=57%) are obtained in an LC/MS purity of 82%. The crude product is used directly for the following steps. ([M+H]+): 327. RT=4.28 min (acetonitrile/water gradient from 30% to 90%-Method B).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08420824B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-f3b74c04fcb2418081506cda1a17ca50
Quellennotizuspto-grants-2013_04