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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 446267Erstellt: 24. Oktober 2026

Hydrochloric Acid → HCID 58396412, Verbindung

https://huagongshe.com/de/reaction/446267

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPhosphorus trichlorideHCID 24387—
Edukt3-Hydroxy-4-methylbenzoic acidHCID 68512—
EduktN-(2-Amino-4-(trifluoromethyl)phenyl)morpholineHCID 136624—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelSodium chloride; waterHCID 57417360—
ProduktHCID 58396412HCID 58396412—

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

3-Hydroxy-4-methylbenzoic acid (530 mg, 3.5 mmol), 3-amino-4-(4-morpholino)benzotrifluoride (890 mg, 3.6 mmol), and DMAP (150 mg, 1.3 mmol) were suspended in 20 mL dry toluene in a 2-neck flask with an attached Dean-Stark trap under N2. The mixture was stirred in a 130° C. oil bath and brought to a boil before PCl3 (0.18 mL, 2 mmol) was added dropwise by glass/Teflon syringe over 15 minutes. Heating was continued an additional 45 minutes. After cooling, the mixture was diluted with brine and ethyl acetate, and acidified with 1 N HCl. After extraction, the organic layer was dried with Na2SO4, concentrated, and purified by flash chromatography (2% MeOH in CH2Cl2). The isolated material was packed into a small filtration apparatus and rinsed with a small amount of CH2Cl2 to provide the title compound as a white solid. 1H NMR (Varian, 400 MHz, DMSO-d6) d: 9.83 (s, 1H), 9.50 (s, 1H), 8.45 (s, 1H), 7.48 (m, 1H), 7.43 (m, 1H), 7.34 (s, 1H), 7.31 (m, 1H), 7.25 (m, 1H), 3.78 (m, 4H), 2.90 (m, 4H), 2.18 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476434B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-249d05d5ddf14b259dd33d918ce7fb4b
Quellennotizuspto-grants-2013_07