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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48932Erstellt: 23. Oktober 2026

Ethyl 4-bromobenzoate → Ethyl 4-(diethoxyphosphoryl)benzoate

https://huagongshe.com/de/reaction/48932

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 4-bromobenzoateHCID 22043—
EduktDiethylphosphiteHCID 3780918—
Katalysator4-MethylmorpholineHCID 7972—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelAcetonitrileHCID 6342—
ProduktEthyl 4-(diethoxyphosphoryl)benzoateHCID 277369367,9%

Reaktionsschritte

A sealed pressure flask, flushed with N2, containing a mixture of 4-bromo-benzoic acid ethyl ester (2a) (5 g, 0.0218 mol), diethyl phosphite (3.093 mL, 0.024 mol), NMM (2.88 mL, 0.0262 mmol) and Pd(PPh3)4 (2.017 g, 0.00175 mol) in acetonitrile (20 mL) was stirred at ambient temperature for 5-10 min, then heated at 90° C. for 18 hours. The reaction mixture was filtered through celite, and the celite was washed with EtOAc (3×30 mL) until the filtrate showed little or no evidence of product by HPLC. The combined organics were dried over Na2SO4 and concentrated on a rotary evaporator. The desired product was purified by silica gel flash chromatography to give a pale yellow oil (4.24 g). 1H NMR (300 MHz, CDCl3) δ (ppm)) 1.36 (m, 6H), 1.42 (t, J=7 Hz, 3H), 4.16 (m, 4H), 4.42 (q, J=7 Hz, 2H),7.93 (m, 2H), 8.15 (m, 2H). 31P NMR (121 MHz, CDCl3) δ 17.63.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06706699B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-25e853dcf40f456684276b1371248d77
Quellennotizuspto-grants-2004_03