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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 272783Erstellt: 25. Oktober 2026

Hexane → 5-Ethoxy-2-fluorophenol

https://huagongshe.com/reaction/272783

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
EduktTrimethyl borateHCID 8470—
EduktPentamethyldiethylenetriamineHCID 18196—
Edukt4-FluorophenetoleHCID 68018—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Ethoxy-2-fluorophenolHCID 18003370139,2%

Reaktionsbedingungen

Temperatur-60 °C

Reaktionsschritte

To 4-ethoxy-1-fluorobenzene (1.0 g, 7.1 mmol) in THF (8.0 mL) was added freshly distilled N,N,N′,N″,N″-pentamethyldiethylenetriamine (0.8 mL) and 1.6 M n-butyllithium in hexane (5.13 ml, 8.2 mmol) at −78° C. After stirred at −60° C. for 1 h, trimethylborate (0.52 mL, 4.6 mmol) was introduced at −78° C. and the solution was warmed up to rt for 2 h. The reaction was quenched by acetic acid (1.5 ml) at 0° C. After 15 min, 30% hydrogen peroxide (1.2 ml) was introduced and the mixture was stirred from 0° C. to rt overnight. The mixture was extracted by EtOAc (3×30 mL). The combined organic layer was washed by brine, dried over MgSO4, and concentrated. The crude product was purified by column chromatography to give 1.0 g colorless oil of 74A. 1H NMR (400 MHz, CDCl3) δ ppm 1.39 (t, J=6.81 Hz, 3 H) 3.96 (q, J=7.03 Hz, 2H) 5.30 (d, J=2.20 Hz, 1H) 6.28-6.43 (m, 1H) 6.55 (dd, J=7.47, 3.08 Hz, 1H) 6.90-7.01 (m, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456195B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-24aa3e9901cf4bc793e5fc858972cb2d
Quellennotizuspto-grants-2008_11