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

HRID 1084484
Notes
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Reaction equation

HRID 1084484 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 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-methylpropyl-phosphonous acid monohydrate, m.p. 96°-100° C., 31P=+25.8 ppm (D2O).

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  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-5e929b07e6b94d928d7c01f83081b6a3
Source dataset
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05004826

Reaction notes

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