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

Sodium Iodide → 3(S)-benzyloxycarbonylamino-4-cyclohexyl-1-iodobutane-2(R,S)-ol

HRID 478029
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 478029
[CH2:1]([O:8][C:9]([NH:11][C@H:12]([CH:20]1[CH2:22][O:21]1)[CH2:13][CH:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[I-:23].[Na+].C[Si](C)(C)Cl>C(#N)C>[CH2:1]([O:8][C:9]([NH:11][C@@H:12]([CH2:13][CH:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1)[CH:20]([OH:21])[CH2:22][I:23])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 5238Sodium IodideHCID 6397ChlorotrimethylsilaneHCID 14158022(1(S)-benzyloxycarbonylamino-2-cyclohexyl-ethyl)oxirane

Produkt 1

HCID 141580273(S)-benzyloxycarbonylamino-4-cyclohexyl-1-iodobutane-2(R,S)-ol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

42.3 g of (1(S)-benzyloxycarbonylamino-2-cyclohexyl-ethyl)-oxirane are taken up in 200 ml of acetonitrile and the resulting solution is cooled to 0°. After the addition of 20.9 g of sodium iodide, there are added dropwise at 0°, over a period of 30 minutes, 17.7 ml of trimethylchlorosilane. The mixture is stirred at 0°-3° for 40 minutes and then poured onto 700 ml of ice-cold water. The aqueous mixture is extracted with ether, and the organic phase is washed with 750 ml of 5% aqueous sodium thiosulphate solution and 750 ml of saturated, aqueous sodium chloride solution. After drying over sodium sulphate and concentrating by evaporation, an oily mixture of the title compound is obtained which is further processed directly.

Aufarbeitung

  1. temperaturethe resulting solution is cooled to 0°
  2. additionare added dropwise at 0°, over a period of 30 minutes
  3. extractionThe aqueous mixture is extracted with ether
  4. washthe organic phase is washed with 750 ml of 5% aqueous sodium thiosulphate solution and 750 ml of saturated, aqueous sodium chloride solution
  5. dry with materialAfter drying over sodium sulphate
  6. concentrationconcentrating by evaporation
  7. additionan oily mixture of the title compound
  8. customis obtained which

Quellen und Nachweise

ORD-Eintrag
ord-9cc5f47757d94c74b32a9ab348812d3a
Quelldatensatz
uspto-grants-1989_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04889869

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion