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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantisobutyl P-(4-aminobut-2-yl)-P-methyl-phosphinateHCID 23374771—
SolventHydrochloric AcidHCID 313—
Product(3-Amino-1-methyl-propyl)-methyl-phosphinic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05567840
Source datasetuspto-grants-1996_10
ORD IDord-068af91a39184c53838690b3caaa0cc8
Source noteuspto-grants-1996_10