StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Ethanol → 4hydroxy-L-proline ethyl ester hydrochloride

HRID 394417
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 394417
S(Cl)([Cl:3])=O.[OH:5][CH:6]1[CH2:10][NH:9][C@H:8]([C:11]([OH:13])=[O:12])[CH2:7]1.[CH2:14](O)[CH3:15]>>[ClH:3].[CH2:14]([O:12][C:11](=[O:13])[C@@H:8]1[CH2:7][CH:6]([OH:5])[CH2:10][NH:9]1)[CH3:15]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 702EthanolHCID 24386Thionyl ChlorideHCID 69248L-Proline, 4-hydroxy-, cis-

Produkt 1

HCID 127093054hydroxy-L-proline ethyl ester hydrochloride

Versuchsvorschrift

200 mL of absolute ethanol were placed in a 500-mL one-necked round-bottomed flask equipped with an addition funnel. The flask was then cooled in a dry ice/acetone bath, then 17 mL (0.23 mmoles) of thionyl chloride were added from the addition funnel over a 10 minute period. The funnel was removed, and 26.2 g (0.20 mmoles) of 4-hydroxyproline were added in one portion while stirring. The flask was equipped with a reflux condenser and a sodium hydroxide trap, and the mixture was refluxed for two hours. The product was precipitated in ether, isolated by filtration, and washed three times with ether, then it was dried under a stream of nitrogen followed by high vacuum.

Aufarbeitung

  1. customequipped with an addition funnel
  2. temperatureThe flask was then cooled in a dry ice/acetone bath
  3. customThe funnel was removed
  4. customThe flask was equipped with a reflux condenser and a sodium hydroxide trap
  5. temperaturethe mixture was refluxed for two hours
  6. customThe product was precipitated in ether
  7. customisolated by filtration
  8. washwashed three times with ether
  9. customit was dried under a stream of nitrogen

Quellen und Nachweise

ORD-Eintrag
ord-3eb8d0f494364333b92057c4088f6fd1
Quelldatensatz
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06602497B1

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion