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Hydrochloric Acid → 2-Phenyl-2-(pyrrolidin-1-yl)acetic acid hydrochloride

HRID 404630
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 404630
[C:1]1([CH:7]([N:13]2[CH2:17][CH2:16][CH2:15][CH2:14]2)[C:8]([O:10]CC)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:18]>O1CCOCC1>[ClH:18].[C:1]1([CH:7]([N:13]2[CH2:17][CH2:16][CH2:15][CH2:14]2)[C:8]([OH:10])=[O:9])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 313Hydrochloric Acid2×HCID 3568733Ethyl 2-phenyl-2-(pyrrolidin-1-yl)acetate

Produkt 1

HCID 66031122-Phenyl-2-(pyrrolidin-1-yl)acetic acid hydrochlorideAusbeute 79 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

Ethyl 2-phenyl-2-(pyrrolidin-1-yl)acetate (0.31 g, 1.33 mmol) was dissolved in dioxane (11 ml) and 37% HCl (1.09 ml, 13.3 mmol) was added dropwise. The mixture was stirred at reflux overnight. Then 37% HCl (1.09 ml, 13.3 mmol) was added again and the reaction was refluxed for additional 24 hours. The solvent was evaporated, the residue was triturated with acetonitrile (10 ml) and the suspension was filtered on a buckner funnel. The solid was recovered to obtain 2-phenyl-2-(pyrrolidin-1-yl)acetic acid hydrochloride (0.25 g, 79% yield) as a white solid.

Aufarbeitung

  1. temperatureat reflux overnight
  2. temperaturethe reaction was refluxed for additional 24 hours
  3. customThe solvent was evaporated
  4. customthe residue was triturated with acetonitrile (10 ml)
  5. filtrationthe suspension was filtered on a buckner funnel
  6. customThe solid was recovered

Quellen und Nachweise

ORD-Eintrag
ord-b6a6c74acd004fe280572b857281e079
Quelldatensatz
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08748613B2

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