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Ethyl 3-amino-2-(4-methoxyphenyl)propyl(diethoxymethyl)phosphinate → 3-Amino-2-(4-methoxyphenyl)propylphosphonous acid

HRID 1084515
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1084515
[NH2:1][CH2:2][CH:3]([C:17]1[CH:22]=[CH:21][C:20]([O:23][CH3:24])=[CH:19][CH:18]=1)[CH2:4][P:5](C(OCC)OCC)(=[O:9])[O:6]CC>Cl>[NH2:1][CH2:2][CH:3]([C:17]1[CH:22]=[CH:21][C:20]([O:23][CH3:24])=[CH:19][CH:18]=1)[CH2:4][P:5]([OH:6])[OH:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 1

HCID 14362836Ethyl 3-amino-2-(4-methoxyphenyl)propyl(diethoxymethyl)phosphinate

Produkt 1

HCID 100140313-Amino-2-(4-methoxyphenyl)propylphosphonous acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 313Hydrochloric AcidLösungsmittel

Versuchsvorschrift

A solution of 4.6 g of ethyl 3-amino-2-(4-methoxyphenyl)propyl-(diethoxymethyl)phosphinate in 30 ml of 36% aqueous hydrochloric acid is heated to reflux for a period of 1 hour. The reaction mixture is then allowed to cool to room temperature, concentrated under reduced pressure and co-evaporated twice with 20 ml of water under reduced pressure. The crude product is dissolved in 20 ml of water, washed twice with 20 ml of diethyl ether and the aqueous layer is then separated and evaporated under reduced pressure. The crude product is dissolved in 50 ml of ethanol and 5 ml of propylene oxide is added dropwise. The precipitated solid is collected by filtration and dried to give 3-amino-2-(4-methoxyphenyl)propylphosphonous acid (1/2M H2O), m.p. 260°-265° C., 31P=+24.5 ppm (D2O).

Aufarbeitung

  1. temperatureto reflux for a period of 1 hour
  2. concentrationconcentrated under reduced pressure
  3. dissolutionThe crude product is dissolved in 20 ml of water
  4. washwashed twice with 20 ml of diethyl ether
  5. customthe aqueous layer is then separated
  6. customevaporated under reduced pressure
  7. dissolutionThe crude product is dissolved in 50 ml of ethanol
  8. addition5 ml of propylene oxide is added dropwise
  9. filtrationThe precipitated solid is collected by filtration
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-c52f613baf194f199b2a1ec1694f3f62
Quelldatensatz
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05004826

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