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Ethyl 3-amino-2-methylpropyl(diethoxymethyl)phosphinate → 3-Amino-2-methylpropylphosphonous acid monohydrate

HRID 622874
Notes
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Reaction equation

HRID 622874 reaction equation
[NH2:1][CH2:2][CH:3]([CH3:17])[CH2:4][P:5](C(OCC)OCC)(=[O:9])[O:6]CC>Cl>[OH2:6].[NH2:1][CH2:2][CH:3]([CH3:17])[CH2:4][P:5]([OH:9])[OH:6]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 14362817Ethyl 3-amino-2-methylpropyl(diethoxymethyl)phosphinate

Product 1

HCID 867414053-Amino-2-methylpropylphosphonous acid monohydrate

Reagents, catalysts & solvents 1

HCID 313Hydrochloric AcidSolvent

Procedure

A solution of 6.0 g of ethyl 3-amino-2-methylpropyl(diethoxymethyl)phosphinate in 30 ml of 36% aqueous hydrochloric acid is heated to reflux for a period of 7 hours. The reaction mixture is then allowed to cool to room temperature, concentrated under reduced pressure and co-evaporated twice with 10 ml water under reduced pressure and co-evaporated twice with 10 ml of water under reduced pressure. The crude product is dissolved in 50 ml of dry ethanol and 5 ml of propylene oxide is added dropwise. The precipitated solid is collected by filtration and dried to give 3-amino-2-methylpropylphosphonous acid monohydrate, m.p. 96°-100° C., 31P=+25.8 ppm (D2O).

Workup

  1. temperatureto reflux for a period of 7 hours
  2. concentrationconcentrated under reduced pressure
  3. dissolutionThe crude product is dissolved in 50 ml of dry ethanol
  4. addition5 ml of propylene oxide is added dropwise
  5. filtrationThe precipitated solid is collected by filtration
  6. customdried

Sources & evidence

ORD record
ord-568ded0d150d452da6c7c01ba637ea25
Source dataset
uspto-grants-1988_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04772738

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes