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Hydrochloric Acid → HCID 178455687, Verbindung

HRID 1797436
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1797436
[NH2:1][C:2](=O)[CH:3]([F:18])[CH:4]([P:6](C(OCC)OCC)(=[O:10])[O:7]CC)[CH3:5].B.C1COCC1.Cl>C1COCC1>[NH2:1][CH2:2][CH:3]([F:18])[CH:4]([PH:6](=[O:7])[OH:10])[CH3:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 2723981Borane;tetrahydrofuranHCID 9857454Ethyl 3-amino-2-fluoro-1-methyl-3-oxopropyl(diethoxymethyl)phosphinate

Produkt 1

HCID 178455687HCID 178455687, VerbindungAusbeute 18,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To an ice bath cooled solution of ethyl 3-amino-2-fluoro-1-methyl-3-oxopropyl(diethoxymethyl)phosphinate (1.6 g, 5.3 mmol) in THF (15 ml) was added 1 M BH3-THF (12.3 mL, 12.3 mmol) while under an argon atmosphere. After 10 minutes, the solution was heated to reflux for 3 h. The solution was cooled to room temperature and 6 N HCl (100 mL) was added dropwise. The THF was removed by rotovap and another portion of 6 N HCl (100 mL) was added. The mixture was refluxed for 3 h. The solution was cooled, evaporated, co-evaporated with water and then with etanol. The residue was purified ion exchange chromatography (DOWEX® 50WX-8-200, H+ form, 3.5×4.0 cm). The ion exchange resin was prewashed with 2:1 methanol/water. The crude product dissolved in 1:1 methanol/water was loaded onto the column and washed with 1:1 methanol/water. The eluent was changed to 3:1 methanol/concentrated ammonium hydroxide. The appropriate fractions were combined and evaporated to give 150 mg (15%) of a diastereomeric mixture of (3-amino-2-fluoro-1-methylpropyl)phosphinic acid as an oil. Data: 1H NMR (400 MHz, D2O) δ 6.2–7.8 (m, 1H), 4.8–5.2 (m, 1H), 3.2–3.5 (m, 2H), 1.8–2.2 (m, 1H), 1.0–1.2 (m, 3H); MS: m/z=156 (M+H)+.

Aufarbeitung

  1. temperaturethe solution was heated
  2. temperatureto reflux for 3 h
  3. customThe THF was removed by rotovap
  4. additionanother portion of 6 N HCl (100 mL) was added
  5. temperatureThe mixture was refluxed for 3 h
  6. temperatureThe solution was cooled
  7. customevaporated
  8. customThe residue was purified ion exchange chromatography (DOWEX® 50WX-8-200, H+ form, 3.5×4.0 cm)
  9. dissolutionThe crude product dissolved in 1:1 methanol/water
  10. washwashed with 1:1 methanol/water
  11. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-29c5f8ca9fbe42ada7576fa7e70543d1
Quelldatensatz
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07034176B2

Notizen zur Reaktion

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