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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5193Generated: October 25, 2026

Diisopropylamine → Ethyl 2-(4-fluorophenyl)-3-nitropropyl(diethoxymethyl)phosphinate

https://huagongshe.com/reaction/5193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Fluoro-4-(2-nitroethenyl)benzeneHCID 98399—
ReactantEthyl(diethoxymethyl)methylphosphinateHCID 13764418—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductEthyl 2-(4-fluorophenyl)-3-nitropropyl(diethoxymethyl)phosphinateHCID 14362828—

Reaction Steps

To a solution of 5.8 g of diisopropylamine in 40 ml of tetrahydrofuran at -78° C. under an atmosphere of nitrogen are added 35.7 ml of a 1.6M solution of n-butyllithium in hexane. This solution is then stirred for a period of 10 minutes at this temperature, after which time a solution of 10.0 g of ethyl(diethoxymethyl)methylphosphinate in 20 ml of tetrahydrofuran is added. This mixture is then stirred for a period of 1 hour at -78° C. after which time a solution of 7.96 g of 4-fluoro-β-nitrostyrene in 20 ml of tetrahydrofuran is introduced. This mixture is then allowed to warm to room temperature when 40 ml of a saturated ammonium chloride solution is added. The aqueous layer is then extracted with 2×25 ml of diethyl ether and the organic extracts are combined and dried over magnesium sulphate. The solvent is then evaporated under reduced pressure and the crude product chromatographed on silica gel using ethyl acetate as an eluent to give ethyl 2-(4-fluorophenyl)-3-nitropropyl(diethoxymethyl)phosphinate as a viscous oil, 31 p=+42.3 and +41.9 ppm (CDCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05243062
Source datasetuspto-grants-1993_09
ORD IDord-ccb81927c486466b913958dd34a1a9b4
Source noteuspto-grants-1993_09