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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 985042Erstellt: 25. Oktober 2026

Bis(trifluoroacetoxy)iodobenzene → 4-[[3-Methyl-4-(4-trifluoromethylbenzyloxy)phenyl]sulfanyl]-2-propylphenoxy-acetic acid ethyl ester

https://huagongshe.com/reaction/985042

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBis(trifluoroacetoxy)iodobenzeneHCID 102317—
Edukt2-[4-(Trifluoromethyl)benzyloxy]tolueneHCID 11219321—
Edukt4-Mercapto-2-propylphenoxy-acetic acid ethyl esterHCID 20768111—
Lösungsmittel1,1,1,3,3,3-Hexafluoro-2-propanolHCID 13529—
Produkt4-[[3-Methyl-4-(4-trifluoromethylbenzyloxy)phenyl]sulfanyl]-2-propylphenoxy-acetic acid ethyl esterHCID 5912912459,9%

Reaktionsschritte

Compound 4.4 (5.0 g, 19.66 mmol) was dissolved in 1,1,1,3,3,3-hexafluoro-2-propanol (30 mL) under argon atmosphere. To the solution was added compound 4.1 (5.23 g, 19.66 mmol) and [bis(trifluoroacetoxy)iodo]benzene (10.14 g, 23.59 mmol) slowly, while maintaining the reaction temperature between 10° C. and 17° C. After stirring for 15 min, the reaction mixture was concentrated in vacuo to give a residue which was purified using silica gel column chromatography (hexane/EtOAc=20/1) to give 4.5 (6.11 g). 1H NMR (400 MHz) (CDCl3) δ 7.64 (2H, d, J=8.2 Hz); 7.54 (2H, d, J=8.1 Hz); 7.20-7.06 (4H, m); 6.76 (1H, d, J=8.4 Hz); 6.62 (1H, d, J=8.4 Hz); 5.11 (2H, s); 4.60 (2H, s); 4.25 (2H, q, J=7.1 Hz); 2.63-2.56 (2H, m); 2.24 (3H, s); 1.67-1.55 (2H, m); 1.28 (3H, t, J=7.1 Hz); 0.92 (3H, t, J=7.4 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06869975B2
Quelldatensatzuspto-grants-2005_03
ORD IDord-38d2925e64434a719c7daf17bfbbfdea
Quellennotizuspto-grants-2005_03