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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1006736Erstellt: 25. Oktober 2026

Ethyl 4-bromobutyrate → Ethyl 4-[(3-hydroxypropyl)phenylamino]butanoate

https://huagongshe.com/reaction/1006736

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 4-bromobutyrateHCID 76300—
Edukt3-(Phenylamino)propan-1-olHCID 410467—
LösungsmittelDiisopropylethylamineHCID 81531—
ProduktEthyl 4-[(3-hydroxypropyl)phenylamino]butanoateHCID 66716979100,8%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 3-(phenylamino)propan-1-ol (Huang, et al., J.Org.Chem.; 58(23):6235-6246(1993)) (65.6 g, 0.43 mol), ethyl 4-bromobutyrate (104.5 g, 0.54 mol) and 100 mL of ethyldiisopropylamine is stirred at 100° C. for 1 h. The reaction is cooled to room temperature and partitioned between water 400 mL and ethyl acetate (500 mL). The organic layer is washed with saturated NaHCO3, brine and dried over Na2SO4. The oil obtained after concentration is chromatographed on silica eluting with 10% EtOH/CHCl3. Concentration of the appropriate fractions affords 115 g (100%) of the desired product as a colorless, viscous oil. 1H NMR (CDCl3) δ 7.23 (m, 2H), 6.72 (m, 3H), 4.14 (q, J=7 Hz, 2H), 3.72 (t, J=6 Hz, 2H), 3.43 (t, 7 Hz, 2H), 3.34 (t, 7 Hz, 2H), 2.35 (t, 7 Hz), 1.88 (m, 4H), 1.26 (t, 7 Hz, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06790945B2
Quelldatensatzuspto-grants-2004_09
ORD IDord-95c11b2babd749d6a794139d62d564b1
Quellennotizuspto-grants-2004_09