HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865836Generated: October 30, 2026
isobutyl P-(4-aminobut-2-yl)-P-methyl-phosphinate → (3-Amino-1-methyl-propyl)-methyl-phosphinic acid
https://huagongshe.com/reaction/865836
Participants
| Role | Name | HCID | Charge |
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| Reactant | isobutyl P-(4-aminobut-2-yl)-P-methyl-phosphinate | HCID 23374771 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | (3-Amino-1-methyl-propyl)-methyl-phosphinic acid | HCID 10219532 | — |
Reaction Steps
A solution of 21.5 g of isobutyl P-(4-aminobut-2-yl)-P-methyl-phosphinate in 80 ml of 36% aqueous hydrochloric acid is heated to reflux for a period of 10 hours. The reaction mixture is then allowed to cool to room temperature, concentrated under reduced pressure, and co-evaporated twice with 100 ml of water. The crude material is dissolved in water, washed with chloroform, and the aqueous layer treated with activated charcoal. The aqueous solution is filtered hot, evaporated to dryness, the crude product is dissolved in 50 ml of methanol and treated with 1-2 ml of propylene oxide. The hygroscopic solid is filtered and triturated with acetone. After drying, P-(4-aminobut-2-yl)-P-methyl-phosphinic acid is obtained as a hygroscopic solid, m.p. 68°-75°, 3P-NMR spectrum: δ=+46.5 ppm (D2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05567840 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-068af91a39184c53838690b3caaa0cc8 |
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| Source note | uspto-grants-1996_10 |
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