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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706203Generated: October 31, 2026

Ammonia → Hydrochloric Acid

https://huagongshe.com/reaction/1706203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactantdiethyl 3-(N-ethoxycarbonyl-N-ethoxycarbonyloxyamino)-2-methylpropylphosphonateHCID 20337240—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHydrochloric AcidHCID 313—
Product3-(N-hydroxyamino)-2-methylpropylphosphonic acidHCID 20337223—

Reaction Steps

A mixture of diethyl 3-(N-ethoxycarbonyl-N-ethoxycarbonyloxyamino)-2-methylpropylphosphonate (28.3 g.). and conc. hydrochloric acid (280 ml.) was refluxed for 18 hours and then concentrated under reduced pressure to give an oily residue. To the residue was added a mixture of water (100 ml.) and ethyl acetate (100 ml.). From the resultant mixture, the aqueous layer was separated, treated with activated charcoal and concentrated under reduced pressure to give an oily residue. The residue was dissolved in a mixture of methanol (30 ml.) and water (15 ml.). The solution was adjusted to pH 4.0 with aqueous ammonia under ice-cooling and concentrated under reduced pressure to give a residue, which was passed through a column of anion exchange resin, Amberlite IRA-400 (OH-form). The column was washed with water and then the object compound was eluted with 1 N hydrochloric acid. The eluate was concentrated under reduced pressure to give oily hydrochloric acid salt of 3-(N-hydroxyamino)-2-methylpropylphosphonic acid (9.6 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04206156
Source datasetuspto-grants-1980_06
ORD IDord-7dbda69016c14933bc8c88491912c831
Source noteuspto-grants-1980_06