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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600603Generated: November 3, 2026

Hydrochloric Acid → HCID 178527054, compound

https://huagongshe.com/reaction/1600603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantEthyl phosphorochloriditeHCID 68530—
ReactantHCID 178419670HCID 178419670—
ProductHCID 178527054HCID 17852705453%

Reaction Conditions

Temperature5 °C

Reaction Steps

Diethylchlorophosphite (15.7 g, 0.1 mol) in 50 mL of dry diethyl ether was cooled to 5° C. under an atmosphere of nitrogen. Phenethylmagnesium bromide (100 mL, 0.1 mol, 1.0 M solution of in Et2O) was added dropwise over 2 hours while maintaining a temperature between 0-10° C. A thick white slurry formed and was stirred for an additional 30 minutes. The mixture was filtered under a nitrogen atmosphere and the filtrate evaporated under reduced pressure to give a clear and colorless liquid. To the liquid was added 20 mL of water followed by 0.5 ml of concentrated hydrochloric acid. An exothermic reaction was observed and stirring continued for 20 minutes followed by extraction with ethyl acetate. The organics were combined, washed with brine, dried (MgSO4) and evaporated. To the clear liquid was added sodium hydroxide (40 mL, 2.0 M NaOH), the resulting solution stirred for 1 hour and then washed with diethyl ether. The aqueous layer was acidified to pH 1.0 with concentrated hydrochloric acid and extracted twice with ethyl acetate. The organics were combined, dried (MgSO4) and evaporated to give 3-phenylpropylphosphinic acid (1, R=CH2CH2CH2Ph, R1 =H) (9.8 g, 53%) as a clear and colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977090
Source datasetuspto-grants-1999_11
ORD IDord-a7944668b0054183a983e029d9d98e83
Source noteuspto-grants-1999_11