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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719246Generated: October 25, 2026

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

https://huagongshe.com/reaction/719246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-bromobenzoateHCID 22043—
ReactantDiethylphosphiteHCID 3780918—
Catalyst4-MethylmorpholineHCID 7972—
CatalystHCID 178418397HCID 178418397—
SolventAcetonitrileHCID 6342—
ProductEthyl 4-(diethoxyphosphoryl)benzoateHCID 277369367.9%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132427B2
Source datasetuspto-grants-2006_11
ORD IDord-3064727042e44329b252a2bcc36b12cb
Source noteuspto-grants-2006_11