HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849025Generated: October 30, 2026
Hydrochloric Acid → HCID 178527054, compound
https://huagongshe.com/reaction/849025
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl phosphorochloridite | HCID 68530 | — |
| Reactant | HCID 178418471 | HCID 178418471 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178527054 | HCID 178527054 | 53.2% |
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. Phenylpropylmagnesium 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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06011021 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-eadc256e3bac424e96c9a78d2261f91e |
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| Source note | uspto-grants-2000_01 |
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