Hydrochloric Acid → 3-Amino-2-hydroxy-propyl(ethyl)phosphinic acid hydrochloride

HRID 2050726Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2050726
C1(=O)[N:5]([CH2:6][CH:7]([O:16][Si](C)(C)C)[CH2:8][P:9]([CH2:14][CH3:15])(=[O:13])[O:10]CC)C(=O)C2=CC=CC=C12.[ClH:27]>>[ClH:27].[NH2:5][CH2:6][CH:7]([OH:16])[CH2:8][P:9]([CH2:14][CH3:15])(=[O:10])[OH:13]

Komponenten

3

Edukt 2

HCID 313Hydrochloric AcidHCID 19090885Ethyl 3-phthalimido-2-trimethylsilyloxy-propyl(ethyl)phosphinate

Produkt 1

HCID 856311253-Amino-2-hydroxy-propyl(ethyl)phosphinic acid hydrochloride

Versuchsvorschrift

A solution of 6.4 g of ethyl 3-phthalimido-2-trimethylsilyloxy-propyl(ethyl)phosphinate in 100 ml of concentrated aqueous hydrochloric acid is heated to reflux for 20 hours. After this time the suspension is cooled to room temperature and filtered. The filtrate is evaporated to dryness, the resulting semi-solid is co-evaporated with water (5×50 ml) and absolute ethanol (5×100 ml) and the white solid is dried in high vacuum overnight. Crystallisation from absolute ethanol/acetone affords 3-amino-2-hydroxy-propyl(ethyl)phosphinic acid hydrochloride, m.p. 114-115°.

Aufarbeitung

  1. temperatureto reflux for 20 hours
  2. filtrationfiltered
  3. customThe filtrate is evaporated to dryness
  4. customthe white solid is dried in high vacuum overnight
  5. customCrystallisation from absolute ethanol/acetone

Quellen und Nachweise

ORD-Eintrag
ord-5250b3b0e4a94eeb81efdbe33ec5df04
Quelldatensatz
uspto-grants-1991_05
Patentnummer
US05013863

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