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DL-alanine → (2S)-2-propanamidopropanoic acid

HRID 1007146
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1007146
C[Si](Cl)(C)C.[NH2:6][CH:7]([C:9]([OH:11])=[O:10])[CH3:8].C(N(CC)CC)C.[C:19](Cl)(=[O:22])[CH2:20][CH3:21]>ClCCl.O>[NH3:6].[C:19]([NH:6][C@H:7]([C:9]([OH:11])=[O:10])[CH3:8])(=[O:22])[CH2:20][CH3:21]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 602DL-alanineHCID 6397ChlorotrimethylsilaneHCID 8471TriethylamineHCID 62324Propionyl chloride

Produkt 2

HCID 222AmmoniaHCID 22788191(2S)-2-propanamidopropanoic acidAusbeute 146,6 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel
HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

Trimethylsilyl chloride (52.4 ml, 0.41 mol) was added dropwise to an ice-cooled solution of D,L-alanine (16.71 g, 0.188 mol) and triethylamine (57.5 ml, 0.41 mol) in dichloromethane (190 ml). Once addition was complete, the solution was stirred at room temperature for 1 h, followed by 1 h at 40° C. The solution was then cooled to −10° C., propionyl chloride (16.29 ml, 0.188 mol) was added dropwise over 15 minutes and, once addition was complete, the reaction was stirred at −10° C. for 2 h, then 16 h at room temperature, before cooling in an ice-bath. Water (100 ml) was added, the mixture was stirred for 15 minutes, then the phases separated. The aqueous layer was evaporated under reduced pressure and the residue triturated with acetone. The resulting solid was filtered off, and the filtrate concentrated under reduced pressure, to give an oil. This oil was purified by column chromatography using DCM:MeOH:0.88 NH3(aq) (89:10:1) as eluant, to give the title compound (20 g; containing 33% triethylamine).

Aufarbeitung

  1. additionOnce addition
  2. waitfollowed by 1 h at 40° C
  3. temperatureThe solution was then cooled to −10° C.
  4. additiononce addition
  5. stirringthe reaction was stirred at −10° C. for 2 h
  6. temperature16 h at room temperature, before cooling in an ice-bath
  7. stirringthe mixture was stirred for 15 minutes
  8. customthe phases separated
  9. customThe aqueous layer was evaporated under reduced pressure
  10. customthe residue triturated with acetone
  11. filtrationThe resulting solid was filtered off
  12. concentrationthe filtrate concentrated under reduced pressure
  13. customto give an oil
  14. customThis oil was purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-2cd6994aa0584030b1a71739577c22eb
Quelldatensatz
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06794387B2

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