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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30553Erstellt: 24. Oktober 2026

Water → 1-{[4-(Difluoromethoxy)phenyl]ethynyl}-3-propylbenzene

https://huagongshe.com/de/reaction/30553

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylboraneHCID 7357—
EduktSodium HydroxideHCID 14798—
EduktN-[(E)-[3-[2-[4-(difluoromethoxy)phenyl]ethynyl]phenyl]methylideneamino]-4-methylbenzenesulfonamideHCID 59790336—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-{[4-(Difluoromethoxy)phenyl]ethynyl}-3-propylbenzeneHCID 5743585689%

Reaktionsschritte

A mixture of N′-[(1E)-(3-{[4-(difluoromethoxy)phenyl]ethynyl}phenyl)methylene]-4-methylbenzenesulfonohydrazide (0.67 mg, 1.52 mmol) in THF was treated with triethyl borane (1.0 M in THF, 1.52 mL, 1.52 mmol), stirred for 2 minutes, treated with NaOH (2.5 N, 0.61 mL, 1.52 mmol), refluxed for 2 hours, cooled to room temperature, poured into water and extracted with EtOAc. The organic extracts were combined, dried over MgSO4 and concentrated in vacuo. The resultant residue was purified on silica gel (ISCO) using hexanes/EtOAc (50/1) as the eluting solvents to give 1-{[4-(difluoromethoxy)phenyl]ethynyl}-3-propylbenzene as a clear oil (386 mg, 89% yield), MS m/e (M+H)+ 286; 1H NMR (400 MHz, DMSO-d6) 0.85 (t, J=7.32 Hz, 3H), 1.57 (m, 2H), 2.6 (t, J=7.32 Hz, 2H), 7.2 (m, 3H), 7.35-7.45 (m, 4H), 7.58 (d, J=8.79 Hz, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423158B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-2afa4f797d6842c69a7d8f1808c9d185
Quellennotizuspto-grants-2008_09