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

HRID 2209926
Notes
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Reaction equation

HRID 2209926 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-methylpropylphosphonous acid monohydrate, m.p. 96°-100° C. 31 p=+25.8 pp, (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-aaabf4a4a8a04e7a8b54eeefa0088e17
Source dataset
uspto-grants-1995_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05457095

Reaction notes

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