HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5172Generated: October 29, 2026
Ethyl 3-amino-l-(4-chlorophenyl)propyl(diethoxymethyl)phosphinate → 3-Amino-1-(4-chlorophenyl)propylphosphonous acid
https://huagongshe.com/reaction/5172
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 3-amino-l-(4-chlorophenyl)propyl(diethoxymethyl)phosphinate | HCID 14362810 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 3-Amino-1-(4-chlorophenyl)propylphosphonous acid | HCID 19379617 | — |
Reaction Steps
A solution of 17.9 g of ethyl 3-amino-1-(4-chlorophenyl)propyl(diethoxymethyl)phosphinate in 200 ml of 36% aqueous hydrochloric acid is heated to reflux for a period of 6 hours. The reaction mixture is then allowed to cool to room temperature, concentrated under reduced pressure and co-evaporated twice with 50 ml of water under reduced pressure. The crude product is then dissolved in 50 ml of water, washed twice with 20 ml of diethyl ether and the aqueous layer is then separated and evaporated under reduced pressure. The crude product is then dissolved in 50 ml of ethanol and 5 ml of propylene oxide is added dropwise. The precipitated solid is collected by filtration and dried to give 3-amino-1-(4-chlorophenyl)propylphosphonous acid, m.p. 210°-220° C., 31P=+29.6 ppm (D2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05243062 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-2d1131dab45645f4ab0bcc2a3bb89e9f |
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| Source note | uspto-grants-1993_09 |
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