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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48078Erstellt: 24. Oktober 2026

Triethylamine → 2,2,2-Trifluoro-1-[[(3-fluoro-phenyl)[3-(trifluoromethyl)benzoyl]amino]methyl]ethyl 3-trifluoromethyl-benzoate

https://huagongshe.com/de/reaction/48078

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
Edukt3-[(3-Fluorophenyl)amino]-1,1,1-trifluoro-2-propanolHCID 11138733—
LösungsmittelChloroformHCID 6212—
Produkt2,2,2-Trifluoro-1-[[(3-fluoro-phenyl)[3-(trifluoromethyl)benzoyl]amino]methyl]ethyl 3-trifluoromethyl-benzoateHCID 1095191473,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

The 3-[(3-fluorophenyl)amino]-1,1,1-trifluoro-2-propanol (446 mg, 2.0 mmol) from EX-662A and triethylamine (544 mg) were dissolved in anhydrous CHCl3 (30 mL) and cooled to 0° C. Then a solution of 3-trifluoromethylbenzoyl chloride (1.04 g, 5.0 mmol) in anhydrous CHCl3 (6 mL) was added over a period of 15 min. The solution was stirred at room temperature. After 14 h, the solution was washed with 5% NaHCO3 (2×20 mL) and brine (2×10 mL), and then dried over anhydrous MgSO4. Removal of the solvent in vacuo gave 832 mg (73%) of the desired 2,2,2-trifluoro-1-[[(3-fluoro-phenyl)[3-(trifluoromethyl)benzoyl]amino]methyl]ethyl 3-trifluoromethyl-benzoate product as an amber oil, which was greater than 95% pure by reverse phase HPLC analysis. 1H NMR (CDCl3) δ7.25-8.39 (m, 9H), 7.02 (q, 1H), 6.71 (m, 2H), 6.11 (m, 1H), 4.58 (dd, 1H), 4.35 (dd, 1H). 19F NMR (CDCl3) δ−64.4 (m, 6F), −77.4 (s, 3F), −111.3 (m, 1F). HRMS calcd. for C25H15F10NO3: 568.0970 [M+H]+, found: 568.0968.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699898B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-c74cdf4c5ca84d5e928b959b06210e26
Quellennotizuspto-grants-2004_03