Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726051Generated: October 26, 2026

4-Nitrophenol → 4-Nitrophenyl P-methyl-P-phenylphosphinate

https://huagongshe.com/reaction/1726051

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantMethyl(phenyl)phosphinoyl chlorideHCID 21983—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Nitrophenyl P-methyl-P-phenylphosphinateHCID 11479699.9%

Reaction Steps

The methylphenylphosphinic acid 4-nitrophenyl ester is prepared in the following way: A suspension of 173 mg of NaH at 50% in oil, in 2 ml of anhydrous tetrahydrofuran, is stirred at ambient temperature under argon. A solution of 500 mg of 4-nitrophenol in 2 ml of anhydrous tetrahydrofuran is added dropwise at ambient temperature. After stirring for approximately 1 hour at ambient temperature, a solution of 630 mg of methylphenylphosphinic chloride in 2 ml of anhydrous tetrahydrofuran is added dropwise over about ten minutes. After stirring for approximately 2 hours, the reaction medium is diluted with 20 ml of distilled water and the aqueous phase is extracted with 2×20 ml of dichloromethane. The combined organic phases are dried over magnesium sulfate, filtered, and concentrated under reduced pressure in a rotary evaporator. 995 mg of methylphenylphosphinic acid 4-nitrophenyl ester are obtained with a purity of 50%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491710B2
Source datasetuspto-grants-2009_02
ORD IDord-bcd5ba3fa5654a029e4f5bcc3b1d88c4
Source noteuspto-grants-2009_02